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WALMART DAYTIME AND NIGHTTIME MS SEVERE RELIEF VALUE PACK Acetaminophen, Dextromethorphan HBr, Diphenhydramine HCl Kit — NDC 79903-0350-12 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

WALMART DAYTIME AND NIGHTTIME MS SEVERE RELIEF VALUE PACK Acetaminophen, Dextromethorphan HBr, Diphenhydramine HCl Kit — NDC 79903-350-12 (Billing 79903-0350-12)

by WAL-MART STORES INC · 1 KIT in 1 CARTON * 6 PACKET in 1 CARTON / 1 POWDER, FOR SOLUTION in 1 PACKET * 6 PACKET in 1 CARTON / 1 POWDER, FOR SOLUTION in 1 PACKET

This is a package of WALMART DAYTIME AND NIGHTTIME MS SEVERE RELIEF VALUE PACK Acetaminophen, Dextromethorphan HBr, Diphenhydramine HCl Kit from WAL-MART STORES INC, marketed since Feb 2026 and currently FDA-listed. It is this product's only package size.

NDC 79903-0350-12
🏷️ FDA NDC (as labeled) 79903-350-12 billing pads the product segment with a zero
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 1, 2026 · this listing last changed Sep 17, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →

This page is curated, coded, and maintained by

Compiled from public FDA, CMS, DailyMed, NADAC, and related drug data sources. Editorial policy

NDC database record

One package, one record: these facts belong to NDC 79903-350-12 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
79903 labeler · 350 product · 12 package
Package marketed since
Feb 2, 2026
Sample package
No — commercial package
Listing certified through
Dec 31, 2027
Barcode (UPC-A, from the NDC)
3 7990335012 4
FDA record last changed
Sep 17, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 79903-350-12
Product NDC 79903-350
11-digit billing NDC 79903035012
RxCUI 2670598, 2670677, 2679420, 2679425, 2679426
Application # M012
SPL Set ID 888bd90a-a059-4814-bd65-6b735ecfaf3a
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2026-02-02
Dosage form KIT
Quick answers
  • RxCUI (RxNorm): 2670598
Why two NDCs? The FDA registers this code as 79903-350-12 — a 5-3-2 layout, and that's what's printed on the package and shown on DailyMed. For insurance claims, every NDC is standardized to a uniform 11-digit 5-4-2 format by adding a zero to the product segment → 79903-0350-12. Same drug, same package — only the format differs.
Where does this data come from?
Identifiers from the FDA openFDA NDC Directory and Structured Product Labeling; RxCUI from RxNorm (NLM); GPI from Medi-Span; GCN / HIC / AHFS / legend from First Databank.

RxNorm drug class

This medicine belongs to the Anilides class.

Drug family (ATC) Anilides
Where does this data come from?
Therapeutic classes from RxNorm RxClass (U.S. National Library of Medicine) — Established Pharmacologic Class (FDA), ATC drug family (WHO) and mechanism of action, matched by this product’s RxCUI.

Clinical

🧪 What is this product?

This kit contains two over-the-counter products formulated to address multiple cold and flu symptoms. The daytime product typically includes acetaminophen for pain and fever relief and dextromethorphan, a cough suppressant. The nighttime product combines acetaminophen with diphenhydramine, an antihistamine commonly used to help reduce symptoms and promote sleep. These are monograph drugs, meaning they are marketed according to FDA category rules for nonprescription cold and cough products.

Supplement & herbal interactions

🌿 Drug–supplement interaction checker →
Where does this data come from?
Plain-language summary from MedlinePlus (U.S. National Library of Medicine); supplement & herbal interactions and nutrient depletion data from the Natural Medicines database; our full guide is HelloPharmacist editorial content.

Pricing

A drug doesn't have one price. Each row is a different public payment system, and none is what you'd pay at the counter — that depends on your insurance. The ⓘ on each row explains what it measures.

Price systemPer eachPer package
Retail pharmacies payNADAC · weekly Not in the retail survey — common for institutional, discontinued, or low-volume packs.
Medicaid paysCMS SDUD · 12 mo No recent Medicaid claims on file for this NDC — rare and low-volume NDCs are suppressed in the public data.
Medicare drug plans payPart D · quarterly No Part D plan price is available for this NDC in our data.
ℹ️
No price is published for this exact package yet. CMS surveys NADAC per package size, so a different pack of the same drug often has one.
Where does this data come from?
NADAC (National Average Drug Acquisition Cost) is the CMS weekly pharmacy-acquisition-cost survey — what pharmacies pay. ASP (Average Sales Price) is the CMS Medicare Part B drug-payment file, published quarterly. Medicaid pays is computed by us from CMS State Drug Utilization Data (total reimbursed ÷ units, trailing 12 months) — gross of rebates and inclusive of dispensing fees, so it reflects what Medicaid paid, not an acquisition cost. Medicare drug plans pay is the median negotiated point-of-sale unit cost across plans listing this NDC in the CMS quarterly Prescription Drug Plan pricing files, before rebates. The VA pays is the federal contract price (FSS, and the statutory Big 4 ceiling where listed) from the VA National Acquisition Center pharmaceutical price file. All are free public government data; each measures a different payer, so the figures are not directly comparable.

Packaging — all sizes for this product

Package NDCDescription Marketing startMarketing endStatus
79903-0350-12 You're viewing this Main listing 1 KIT in 1 CARTON * 6 PACKET in 1 CARTON / 1 POWDER, FOR SOLUTION in 1 PACKET * 6 PACKET in 1 CARTON / 1 POWDER, FOR SOLUTION in 1 PACKET 2026-02-02 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Theraflu Severe Cold Relief Combo Pack 00067-0123-01 Haleon 1 kit — — FDA listed —
Theraflu Severe Cold Relief Combo Pack 00067-0122-01 Haleon 1 kit — — FDA listed —
Walmart Daytime And Nighttime Ms Severe Relief Value Packthis 79903-0350-12 WAL-MART 1 kit — — FDA listed —
Vicks DayQuil NyQuil HOT REMEDY Cold and Flu 58933-0556-06 Procter 1 kit — — FDA listed —
Vicks DayQuil NyQuil HOT REMEDY Cold and Flu 58933-0554-06 Procter 1 kit — — Discontinued —
Daytime and Nighttime Kids Multi-Symptom Cold and Flu combo pack 69676-0092-03 Genexa 2 bottles — — FDA listed —
About this product: other versions of the same ingredient, strength and form are listed above, least expensive first, with FDA equivalence ratings where available.
Where does this data come from?
Equivalents are other NDCs of the same ingredient, form and route from the openFDA NDC Directory, ranked least-expensive-first by NADAC. Therapeutic-equivalence (AB) ratings come from the FDA Orange Book; biologics use the FDA Purple Book for biosimilar & interchangeable status.

Availability & generic status

🏛️
2026
On the market since
Feb 2026
📍
2026
Currently FDA-listed
listed with the FDA
🔒
·
No generic listed yet
brand only
ℹ️No FDA-approved generic found

We did not find an FDA-approved generic match for this exact strength, form and route.

Where does this data come from?
Patents and exclusivity from the FDA Orange Book (small-molecule drugs), refreshed from public FDA data. Generic launch timing is an estimate, not a guarantee.

Inactive Ingredients / Excipients

Inactive ingredients, also called excipients, are components of the drug product other than the active ingredient. They may include fillers, dyes, coatings, preservatives, flavors, or other formulation ingredients.

From the label’s inactive-ingredient sectionanhydrous citric acid, caramel, flavors, maltodextrin, potassium chloride, silica, sucralose, sucrose anhydrous citric acid, F D & C yellow #6, flavors, maltodextrin, potassium chloride, silica,sucralose, sucrose,

This is label-wide narrative text, not a normalized exact-product ingredient list. A label can cover multiple strengths or packages.

Where does this data come from?
Source: official FDA Structured Product Labeling (SPL) via DailyMed and the openFDA label index. Structured IACT rows and label-wide narrative are kept separate; availability and product-level specificity depend on the submitted label.

Inactive ingredient FAQ

Are inactive ingredients the same for every manufacturer?
No. Inactive ingredients can differ by manufacturer, dosage form, strength, and package / product version.
Why might an inactive ingredient be missing?
Some SPLs do not provide a complete structured inactive-ingredient list, and older or unusual labels may only include the information in narrative text.
Can inactive ingredients matter?
Yes. They can matter for allergies, intolerances, dyes, gluten / lactose concerns, preservatives, and formulation differences — but confirm with a pharmacist or the manufacturer when it’s clinically important.

Manufacturer & labeler

LabelerWAL-MART STORES INC
FDA applicationM012 (OTC MONOGRAPH DRUG)
Labeler code79903
First marketedFeb 2026
Product typeHuman Otc Drug
Portfolio199 products on file

More NDCs from WAL-MART STORES INC labeler code 79903

The labeler markets the product; the application holder owns the FDA approval. They’re often the same company but can differ (e.g. a repackager or an authorized generic). A mailing address / phone appears here when the manufacturer includes it in the product’s FDA label (not all do).
Where does this data come from?
Labeler, application holder and registered establishment from the FDA openFDA NDC Directory and Drugs@FDA; address/contact from the product’s FDA label.

FDA label — Drug Facts FDA SPL

The complete FDA label for this product — the official Drug Facts labeling, verbatim, section by section. Jump with a chip, search within the label, or expand everything.
🎯 Indications and Usage ⏱️ Dosage and Administration ⚠️ Warnings 📦 Storage and Handling 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose 📄 Do Not Use 📄 Ask a Doctor Before Use If 📄 Ask a Doctor or Pharmacist Before Use If 📄 When Using This Product 📄 Stop Use and Ask a Doctor If 🤰 If Pregnant or Breast-Feeding 📄 Keep Out of Reach of Children 📄 Questions or Comments 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 98 words ▾

Uses - Daytime Severe Cold Relief ▪ temporarily relieves these symptoms due to a cold: ▪ minor aches and pains ▪ minor sore throat pain ▪ headache ▪ cough due to minor throat and bronchial irritation ▪ temporarily reduces fever

Uses - Nighttime Severe Cold Relief ▪ temporarily relieves these symptoms due to a cold: ▪ minor aches and pains ▪ minor sore throat pain ▪ headache ▪ runny nose ▪ sneezing ▪ itchy nose or throat ▪ itchy, watery eyes due to hay fever ▪ cough due to minor throat and bronchial irritation ▪ temporarily reduces fever

⏱️ Dosage and Administration ~1 min read ▾

Directions – Daytime Severe Cold Relief ▪ do not use more than directed ▪ take every 4 hours, while symptoms persist. Do not take more than 6 packets in 24 hours unless directed by a doctor Age Dose Adults and children 12 years of age and over One packet Children under 12 years of age Do not use ▪ dissolve contents of one packet into 8 oz. hot water: sip while hot. Consume entire drink within 10 - 15 minutes. ▪ if using a microwave, add contents of one packet to 8 oz. of cool water: stir briskly before and after heating, Do not overheat Directions Nighttime Severe Cold Relief ▪ do not use more than directed ▪ take every 4 hours while symptoms persist, Do not take more than 5 packets in 24 hours unless directed by a doctor Age Dose Adults and Children 12 years of age and over One packet Children under 12 years of age do not use ▪ dissolve contents of one packet into 8 oz. hot water: sip while hot.

Consume entire drink within 10 - 15 minutes. ▪ if using a microwave, add contents of one packet to 8 oz. of cool water: stir briskly before and after heating, Do not overheat.

Directions Nighttime Severe Cold Relief ▪ do not use more than directed ▪ take every 4 hours while symptoms persist, Do not take more than 5 packets in 24 hours unless directed by a doctor Age Dose Adults and Children 12 years of age and over One packet Children under 12 years of age do not use ▪ dissolve contents of one packet into 8 oz. hot water: sip while hot. Consume entire drink within 10 - 15 minutes. ▪ if using a microwave, add contents of one packet to 8 oz. of cool water: stir briskly before and after heating, Do not overheat.

⚠️ Warnings 114 words ▾

Warnings – Daytime Severe Cold Relief /Nighttime Severe Cold Relief Liver warning : This product contains acetaminophen. Severe liver damage may occur if you take ▪ more than 4,000 mg of acetaminophen in 24 hours ▪ with other drugs containing acetaminophen ▪ 3 or more alcoholic drinks every day while using this product Allergy alert: Acetaminophen may cause severe skin reactions. Symptoms may include: ▪ skin reddening ▪ blisters ▪ rash If a skin reaction occurs, stop use and seek medical help right away Sore throat warning : If sore throat is severe, persists for more than 2 days, is accompanied or followed by fever, headache, rash, nausea, or vomiting, consult a doctor promptly.

📦 Storage and Handling 62 words ▾

Other information - Daytime Severe Cold Relief ▪ each packet contains : potassium 6 mg ▪ Aspartame free, sodium free ▪ store at room temperature. Protect from excessive heat and moisture.

Other information - Nighttime Severe Cold Relief ▪ each packet contains : potassium 6 mg ▪ Aspartame free, sodium free ▪ store at room temperature. Protect from excessive heat and moisture

🧪 Active Ingredient 34 words ▾

Active ingredients (in each packet) – Daytime Severe Cold Relief Acetaminophen 500 mg Dextromethorphan hydrobromide 20 mg

Active ingredients (in each packet) - Nighttime Severe Cold Relief Acetaminophen 650 mg Diphenhydramine hydrochloride 25 mg

🧪 Inactive Ingredients 42 words ▾

Inactive ingredients - Daytime Severe Cold Relief anhydrous citric acid, caramel, flavors, maltodextrin, potassium chloride, silica, sucralose, sucrose

Inactive ingredients - Nighttime Severe Cold Relief anhydrous citric acid, F D & C yellow #6 , flavors, maltodextrin, potassium chloride, silica ,sucralose, sucrose,

🎯 Purpose 22 words ▾

Purpose - Daytime Severe Cold Relief Pain reliever/fever reducer Cough Suppressant

Purpose - Nighttime Severe Cold Relief Pain reliever/fever reducer Antihistamine/Cough suppressant

📄 Do Not Use 218 words ▾

Do not use - Daytime Severe Cold Relief ▪ in a child under 12 years of age ▪ if you are allergic to acetaminophen ▪ with any other drug containing acetaminophen (prescription or nonprescription). If you are not sure whether a drug contains acetaminophen, ask a doctor or a pharmacist. ▪ if you are now taking a prescription monoamine oxidase inhibitor (MAOI) (certain drugs for depression, psychiatric, or emotional conditions, or Parkinson's disease), or for 2 weeks after stopping the MAOI drug. If you do not know if your prescription drug contains an MAOI, ask a doctor or pharmacist before taking this product.

Do not use - Nighttime Severe Cold Relief ▪ in a child under 12 years of age ▪ if you are allergic to acetaminophen ▪ with any other drug containing acetaminophen (prescription or nonprescription). If you are not sure whether a drug contains acetaminophen, ask a doctor or a pharmacist. ▪ with any other product containing diphenhydramine, even one used on skin ▪ if you are now taking a prescription monoamine oxidase inhibitor (MAOI) (certain drugs for depression, psychiatric, or emotional conditions, or Parkinson’s disease), or for 2 weeks after stopping the MAOI drug.

If you do not know if your prescription drug contains an MAOI, ask a doctor or pharmacist before taking this product.

📄 Ask a Doctor Before Use If 101 words ▾

Ask a doctor before use if you have - Daytime Severe Cold Relief ▪ liver disease ▪ cough that occurs with too much phlegm (mucus) ▪ cough that lasts or is chronic such as occurs with smoking, asthma, or emphysema

Ask a doctor before use if you have - Nighttime Severe Cold Relief ▪ liver disease ▪ glaucoma ▪ trouble urinating due to an enlarged prostate gland ▪ a breathing problem such as emphysema or chronic bronchitis ▪ cough that occurs with too much phlegm (mucus) ▪ cough that lasts or is chronic such as occurs with smoking, asthma, or emphysema

📄 Ask a Doctor or Pharmacist Before Use If 49 words ▾

Ask a doctor or pharmacist before use if you are - Daytime Severe Cold Relief ▪ taking the blood thinning drug warfarin

Ask a doctor or pharmacist before use if you are - Nighttime Severe Cold Relief ▪ taking sedatives or tranquilizers ▪ taking the blood thinning drug warfarin

📄 When Using This Product 58 words ▾

When using this product - Daytime Severe Cold Relief do not exceed recommended dosage

When using this product - Nighttime Severe Cold Relief ▪ avoid alcoholic drinks ▪ marked drowsiness may occur ▪ alcohol, sedatives, and tranquilizers may increase drowsiness ▪ be careful when driving a motor vehicle or operating machinery ▪ excitability may occur, especially in children

📄 Stop Use and Ask a Doctor If 68 words ▾

Stop use and ask a doctor if – Daytime Severe Cold Relief /Nighttime Severe Cold and Cough fever gets worse or lasts more than 3 days • redness or swelling is present • new symptoms occur • pain, or cough gets worse or lasts more than 7 days • cough comes back or occurs with rash or headache that lasts. These could be signs of a serious condition.

🤰 If Pregnant or Breast-Feeding 10 words ▾

If pregnant or breast-feeding, ask a health professional before use.

📄 Keep Out of Reach of Children 44 words ▾

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away (1-800-222-1222). Prompt medical attention is critical for adults as well as for children even if you do not notice any signs or symptoms.

📄 Questions or Comments 4 words ▾

Questions or comments? 1-866-467-2748

📄 Package Label / Principal Display Panel ~1 min read ▾

Package/Label Principal Display Panel DAYTIME & NIGHTTIME RELIEF VALUE PACK Compare to Theraflu® Multi Symptom Severe Cold Relief active ingredients* Nighttime Severe Cold Relief active ingredients* NDC 79903-350-12 DAYTIME SEVERE MULTI- SYMPTOM COLD RELIEF Acetaminophen - Pain Reliever/ Fever Reducer Dextromethorphan HBr - Cough Suppressant Hot Liquid Therapy That Relieves • Cough • Head & Body • Sore throat pain • ache • Fever Honey Lemon Flavor Infused with chamomile and white tea flavors Naturally and Artificially Flavored 6 PACKETS NIGHTTIME SEVERE MULTI-SYMPTOM COLD Relief Acetaminophen - Pain Reliever/ Fever Reducer Dextromethorphan HBr - Cough Suppressant Hot Liquid Therapy That Relieves • Cough • Head & Body • Sore throat pain • Ache • Runny nose • Sneezing • Fever Honey lemon flavor Infused with chamomile & white tea flavors 6 PACKETS 12 TOTAL PACKETS READ ALL WARNINGS AND DIRECTIONS ON CARTON BEFORE USE .KEEP CARTON FOR REFERENCE, DO NOT DISCARD.

DO NOT TAKE BOTH PRODUCTS AT THE SAME TIME OR TAKE MORE THAN 5 DOSES IN TOTAL IN ANY 24 –HOUR PERIOD. DO NOT TAKE A DOSE OF THE NIGHTTIME PRODUCT SOONER THAN 4 HOURS AFTER THE LAST DOSE OF DAYTIME PRODUCT UNLESS DIRECTED BY DOCTOR. *These Products are not manufactured or distributed by Haleon, owner of Theraflu ® Multi-Symptom Daytime Severe Cold & Theraflu ® Multi-Symptom Nighttime Severe Cold Relief. Distributed By: Wal-Mart Stores, Inc.

Bentonville, AR 72716 © Wal-Mart Stores, Inc. Satisfaction guaranteed – or we’ll replace it or give you your money back. For questions or comments or to report an undesired reaction or side effect, please call 1-888-287-1915 TAMPER EVIDENT INNER UNIT: DO NOT USE IF SEALED PACKET IS TORN OR BROKEN Equate Daytime and Nighttime Relief Value Pack 12 Packets

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗

Reported adverse events (FAERS)

Read carefully: FAERS reports are voluntary and unverified. Counts are not incidence, do not establish causation, are subject to reporting bias, and cannot be used to compare one drug to another. Shown for signal context only. Reports for Acetaminophen, Dextromethorphan HBr, Diphenhydramine HCl — the ingredient across all brands.

Top reported reactions

Dyspnoea8
Fatigue8
Pain8
Nasopharyngitis7
Anxiety6
Feeling Abnormal6
Headache6

Age at onset

Adult5
Elderly2

Reporter sex

81 reports

Serious outcomes

Hospitalization22
Life-threatening6
Death4
Disabling2
Reports over time (by year) — tap or hover for the count & year
2020 2022 2024 2026 7 0
Most recent year is provisional (FAERS lags ~3 months).
Where does this data come from?
Adverse-event reports from the FDA Adverse Event Reporting System (FAERS) via openFDA. FAERS reports are voluntary and unverified — counts are not incidence and don’t establish causation.

About this NDC listing & data coverage

Over-the-counter (OTC) product Kit / multi-component package

Kit / multi-component package

This NDC identifies a kit — a package containing more than one component. Structured data (pricing, ingredients, equivalents) is often reported per component rather than for the kit NDC itself, which can make this page look thinner than the components' own pages.

What data is (and isn’t) available for this NDC — tap to expand
NDC identity (package / product / labeler codes) ✓ Available
Labeler ✓ Available
Product & package description ✓ Available
Marketing category & status ✓ Available
Active ingredient / dosage form / route ✓ Available
FDA label (SPL via DailyMed) ✓ Available
Package photos ✓ Available
Inactive ingredients (structured) ✓ Available
NADAC pharmacy acquisition price (CMS) — Not published for this NDC CMS publishes NADAC only for NDCs reported in its retail-pharmacy survey.
Orange Book / therapeutic-equivalence data — Not published for this NDC Applies only to products approved under an NDA/ANDA; many listings are out of scope.
HCPCS J-code billing crosswalk — Not published for this NDC Most self-administered / retail products have no J-code — that is normal.
Medicaid utilization (CMS SDUD) — Not published for this NDC CMS reports utilization only for NDCs with Medicaid claims above its privacy threshold.
“Not published” reflects what the public FDA / CMS / NLM sources provide for this exact package code — it is a property of the data feeds, not a judgment about the product.

Questions about this listing

Is this NDC FDA-approved?
An NDC listing does not by itself establish FDA approval — the NDC Directory records that a product is listed with FDA, not that it was reviewed and approved. This listing's marketing category is "Otc Monograph Drug". Products approved under an application carry an NDA, ANDA, or BLA number.
Why is there no price listed?
The pricing shown on our NDC pages comes from CMS NADAC, a voluntary survey of retail community pharmacy invoices. CMS does not publish a NADAC for every NDC — packages outside the retail survey (institutional and hospital products, bulk packages, discontinued items, and many OTC items) may never receive one. A missing price reflects the survey's scope, not this product's actual cost, and does not mean the product is free or unavailable.
Is the NDC printed on the package the same as the 11-digit billing NDC?
Yes, they identify this exact package in different formats. The form printed on the packaging and shown on DailyMed is the one the FDA registered. Insurance claims use a fixed 11-digit 5-4-2 format, so the short segment is padded with a leading zero and the dashes are dropped. The Identity section at the top of this page lists each form of this code.
Is this package still being marketed?
Yes, per the latest FDA NDC Directory data on this page: this package is listed as actively marketed, with no marketing end date reported by WAL-MART STORES INC. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
WAL-MART STORES INC is the labeler of record for this NDC — the company under whose FDA-assigned code the package is listed. The labeler may be the manufacturer itself or a distributor marketing the product under its own code.
Do I need a prescription for this product?
This NDC is listed with FDA as an over-the-counter product, so it does not require a prescription. Follow the package directions, and ask your pharmacist if you are unsure whether it is right for you.
This page identifies an FDA-listed package (the NDC) and reports public regulatory and pricing data about the listing. It is reference information, not a medical recommendation — talk to your pharmacist or prescriber about your own medication.
Where does this data come from?
Listing facts (marketing category, packager status, marketing dates) from the FDA openFDA NDC Directory; label availability from DailyMed; pricing coverage from CMS NADAC; equivalence scope from the FDA Orange Book.
← 79903-0349-04 · WALMART 79903-0351-05 · Walmart →
For educational and professional reference only — not medical advice. Pricing reflects published NADAC and CMS ASP (free public data) and may differ from your acquisition cost; always verify before billing or dispensing.