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Docosanol 100 mg/g Cream — NDC 00363-8980-07 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Docosanol 100 mg/g Cream — NDC 0363-8980-07 (Billing 00363-8980-07)

by Walgreens · 1 TUBE in 1 PACKAGE / 2 g in 1 TUBE

This is a package of Docosanol 100 mg/g Cream from Walgreens, marketed since Dec 2023 and currently FDA-listed, this package's marketing is listed to end Dec 2027. It is the main listing for this product, which comes in 2 package sizes.

NDC 00363-8980-07
🏷️ FDA NDC (as labeled) 0363-8980-07 billing pads the labeler segment with a zero
This package
Contains2 g in 1 tube Pack sizes2 compare ↓
Main listing for product 0363-8980 · Also comes in: 2 tubes 0363-8980-14
OTC Generic On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 1, 2026 · this listing last changed Jul 24, 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

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 0363-8980-07
Product NDC 0363-8980
11-digit billing NDC 00363898007
RxCUI 797534
UNII 9G1OE216XY
UPC 0311917197395
Application # ANDA212385
SPL Set ID 1500df4d-0c69-4590-a67f-d11edcccd90c
DEA schedule Non-controlled
Marketing category ANDA
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2023-12-31
Marketing end 2027-12-31
Route TOPICAL
Dosage form CREAM
Substance DOCOSANOL
Quick answers
  • RxCUI (RxNorm): 797534
Why two NDCs? The FDA registers this code as 0363-8980-07 — a 4-4-2 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 labeler segment → 00363-8980-07. 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 Antivirals class.

Drug family (ATC) Antivirals
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

📗 Our plain-language guide HelloPharmacist
  • It treats cold sores, also called fever blisters, on your face or lips. It can shorten healing time and how long tingling, pain, burning and itching last.
  • Start at the very first sign, usually a tingle. Early treatment gives the best results. Wash your hands before and after, then rub it in gently but completely.
  • Adults and children 12 and older use it 5 times a day until the cold sore heals. If your child is under 12, check with a doctor first.
  • It can rarely cause a severe allergic reaction, with hives, facial swelling, wheezing, rash or trouble breathing. If that happens, stop and get medical help right away. Do not use...
📖 Read our full Docosanol guide →

Supplement & herbal interactions

Some supplements/herbs that may interact with Docosanol — tap one for details:

Dimethylsulfoxide (dmso)Moderate Turpentine OilModerate AlchemillaMinor
🌿 Every supplement checked against Docosanol (3 interactions) — ranked by severity →
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 gPer 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.
Try another pack size: 2 tubes
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
00363-8980-07 You're viewing this Main listing 1 TUBE in 1 PACKAGE / 2 g in 1 TUBE 2023-12-31 Dec 31, 2027 Active
00363-8980-14 0363-8980-14 2 TUBE in 1 PACKAGE / 2 g in 1 TUBE 2023-12-31 Dec 31, 2027 Active

Pack size FAQ

What quantity is in this package?
This package is listed by the FDA — 1 tube in 1 package / 2 g in 1 tube.
What NDC number is used to bill for this package of Docosanol 100 mg/g Cream?
Use the 11-digit billing form listed in the identifiers section of this page. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Docosanol 100 mg/g 00536-1427-04 Rugby 1 tube $5.793 — Availability likely —
Docosanol 100 mg/g 00713-0353-02 Cosette 1 tube $5.793 — Availability likely —
Docosanol 100 mg/g 46122-0800-36 Amerisource 1 tube $5.793 — Availability likely —
Docosanol 100 mg/g 51672-1406-02 Sun 2 tubes $5.793 — Availability likely —
Docosanol 100 mg/g 61269-0881-35 H2-Pharma, 2 g $5.793 — Availability likely —
Docosanol 100 mg/g 61269-0989-37 H2-Pharma, 1 bottle $5.793 — Availability likely —
Docosanol 100 mg/g 70000-0672-01 Leader/ 1 tube $5.793 — Availability likely —
Cold Sore Fever Blister Treatment 100 mg/g 70677-1255-01 Strategic 1 tube $5.793 — Availability likely —
Docosanol 100 mg/g 62011-0433-01 Strategic 1 tube $5.946 — FDA listed —
Abreva 100 mg/g 00135-0200-01 Haleon 2 g — — FDA listed —
Abreva 100 mg/g 00135-0300-01 Haleon 1 tube — — FDA listed —
Cold Sore Fever Blister Treatment 100 mg/g 00363-6510-07 Walgreens 2 g — — FDA listed —
Cold Sore Fever Blister Treatment 100 mg/g 00363-8877-07 Walgreens 2 g — — FDA listed —
Docosanol 100 mg/gthis 00363-8980-07 Walgreens 1 tube — — FDA listed —
Cold Sore Fever Blister Treatment 100 mg/g 00363-9220-07 Walgreens 1 tube — — FDA listed —
Cold Sore Fever Blister Treatment 100 mg/g 00363-9222-07 Walgreens 1 tube — — FDA listed —
Cold Sore Treatment Docosanol 100 mg/g 10157-2124-02 Blistex 1 tube — — FDA listed —
Cold Sore Fever Blister Treatment 100 mg/g 11673-0769-14 TARGET 2 tubes — — FDA listed —
Cold Sore Fever Blister Treatment 100 mg/g 11673-0846-14 TARGET 2 tubes — — FDA listed —
Docosanol 100 mg/g 21130-0422-07 Safeway, 1 tube — — Discontinued —
Cold Sore Fever Blister Treatment 100 mg/g 21130-0605-07 Safeway, 2 g — — FDA listed —
Docosanol 100 mg/g 21130-0770-07 Safeway, 1 tube — — FDA listed —
Cold Sore Fever Blister Treatment 100 mg/g 21130-0823-07 Safeway, 1 tube — — FDA listed —
Docosanol 100 mg/g 21922-0023-17 Encube 1 bottle — — FDA listed —
Docosanol 100 mg/g 30142-0286-02 KROGER 1 tube — — FDA listed —
Cold Sore Fever Blister 100 mg/g 30142-0322-07 The 1 tube — — Discontinued —
Cold Sore Fever Blister Treatment 100 mg/g 30142-0869-07 The 2 g — — FDA listed —
Cold Sore Fever Blister Treatment 100 mg/g 30142-0981-07 The 1 tube — — FDA listed —
Cold Sore Fever Blister 100 mg/g 37808-0223-07 H 1 tube — — FDA listed —
Cold Sore Treatment 100 mg/g 37808-0229-07 H 1 tube — — FDA listed —
Cold Sore Fever Blister 100 mg/g 37808-0661-07 H 1 tube — — FDA listed —
Cold Sore Fever Blister Treatment 100 mg/g 37808-0765-07 H 2 g — — FDA listed —
Docosanol 100 mg/g 41163-0724-07 United 1 tube — — FDA listed —
Docosanol 100 mg/g 41250-0867-07 MEIJER, 1 tube — — FDA listed —
Docosanol 100 mg/g 41415-0660-03 Publix 1 tube — — FDA listed —
Docosanol 100 mg/g 46708-0682-01 Alembic 1 tube — — FDA listed —
Docosanol 100 mg/g 49035-0259-35 EQUATE 1 tube — — FDA listed —
Docosanol 100 mg/g 51316-0763-02 CVS 1 tube — — FDA listed —
Docosanol 100 mg/g 55301-0112-07 AAFES/Your 1 tube — — FDA listed —
Docosanol 100 mg/g 55301-0877-07 AAFES/Your 1 tube — — FDA listed —
Docosanol 100 mg/g 55319-0922-07 Family 1 tube — — FDA listed —
Cold Sore Fever Blister Treatment 100 mg/g 55910-0550-07 Dolgencorp, 2 g — — FDA listed —
Cold Sore Fever Blister Treatment 100 mg/g 55910-0859-07 Dolgencorp, 1 tube — — FDA listed —
Cold Sore Fever Blister Treatment 100 mg/g 55910-0963-07 Dolgencorp, 1 tube — — FDA listed —
Docosanol 100 mg/g 58602-0019-08 Aurohealth 1 tube — — FDA listed —
Cold Sore Treatment 100 mg/g 59726-0112-07 P 1 tube — — FDA listed —
Cold Sore Fever Blister 100 mg/g 59726-0221-07 P 1 tube — — FDA listed —
Cold Sore Fever Blister Treatment 100 mg/g 59726-0877-07 P 2 g — — FDA listed —
Cold Sore Treatment 100 mg/g 59726-0922-07 P 1 tube — — FDA listed —
Cold Sore Treatment 100 mg/g 59726-0924-07 P 1 tube — — FDA listed —
Docosanol 100 mg/g 62332-0682-01 Alembic 1 tube — — FDA listed —
Docosanol 100 mg/g 63941-0922-07 Best 1 tube — — FDA listed —
Cold Sore Fever Blister Treatment 100 mg/g 68016-0344-07 Chain 1 tube — — FDA listed —
Docosanol 100 mg/g 70000-0743-01 Leader/ 1 bottle — — FDA listed —
Amazon Basics Docosanol 100 mg/g 72288-0006-01 Amazon.com 1 tube — — FDA listed —
Docosanol 100 mg/g 72476-0492-07 Care 1 tube — — FDA listed —
Docosanol 100 mg/g 72476-0922-07 Care 1 tube — — FDA listed —
Docosanol 100 mg/g 72476-0965-07 Care 1 tube — — FDA listed —
Docosanol 100 mg/g 73581-0004-02 YYBA 2 tubes — — FDA listed —
Cold Sore Fever Blister Treatment 100 mg/g 76162-0818-07 Topco 1 tube — — FDA listed —
Cold Sore Fever Blister Treatment 100 mg/g 76162-0900-07 Topco 1 tube — — FDA listed —
Cold Sore Fever Blister Treatment 100 mg/g 79481-0065-07 Meijer 2 g — — FDA listed —
Cold Sore Fever Blister Treatment 100 mg/g 79481-9220-07 Meijer 2 tubes — — FDA listed —
Docosanol 100 mg/g 79903-0011-07 WALMART 1 tube — — FDA listed —
Docosanol 100 mg/g 79903-0118-14 WALMART 2 tubes — — FDA listed —
Cold Sore Fever Blister Treatment 100 mg/g 79903-0248-07 WALMART 1 tube — — FDA listed —
Docosanol 100 mg/g 79903-0402-10 WALMART 1 tube — — FDA listed —
Cold Sore Fever Blister Treatment 100 mg/g 79903-0435-00 WALMART 2 g — — FDA listed —
Cold Sore Fever Blister Treatment 100 mg/g 81522-0112-07 FSA 1 tube — — FDA listed —
Cold Sore Treatment 100 mg/g 81522-0922-07 FSA 1 tube — — FDA listed —
Cold Sore Fever Blister Treatment 100 mg/g 81522-0923-07 FSA 1 tube — — FDA listed —
Julie Cold Sore Treatment 100 mg/g 82791-0362-01 Julie 2 g — — FDA listed —
Cold Sore Fever Blister Treatment 100 mg/g 85766-0239-02 Sportpharm 1 tube — — FDA listed —
Docosanol 100 mg/g 84725-0001-01 KLM 1 tube — — FDA listed —
Docosanol 100 mg/g 43598-0044-02 Dr.Reddys' 1 tube — — FDA listed —
About this product: this is a generic version of the medicine. FDA equivalence ratings are shown when available, and other versions are listed above, least expensive first.
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

🏛️
2023
On the market since
Dec 2023
📍
2026
Currently FDA-listed
3 years listed
🔓
·
Generic on the market
this product is a generic
✅This is a generic drug

This product is an FDA-approved generic. Other versions of the same drug are listed under Therapeutic equivalents, least expensive first.

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.

What it looks like

Color white
One label can cover several strengths, so colors may be combined — always confirm a loose pill against the dispensed prescription label or a pharmacist.
Where does this data come from?
Physical description (imprint, shape, color, scoring, coating) from this product’s FDA Structured Product Labeling (SPL), mirrored from DailyMed / openFDA.

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.

💡 Tap an ingredient (hover on desktop) to see what it is and why it’s used.

  • UNII LKG8494WBH
    Benzyl alcohol is a clear liquid used as a preservative and solvent in medicines. It helps prevent bacterial and fungal growth and dissolves other ingredients to create uniform liquid formulations.
  • UNII N6K5787QVP
    Light mineral oil is a clear, odorless liquid derived from petroleum. In medicines, it acts as a lubricant and emollient to help the product spread smoothly and improve texture.
  • UNII 6DC9Q167V3
    Propylene glycol is a clear liquid derived from petroleum or vegetable sources. It acts as a solvent, humectant, and preservative in medicines, helping dissolve active ingredients and maintain product stability.
  • UNII 33X4X4B90S
    Sucrose distearate is an emulsifier made from sugar and stearic acid. It helps mix oil and water-based ingredients together and improves the texture and stability of the medicine.
  • UNII 274KW0O50M
    Sucrose stearate is a compound made from sugar and stearic acid (a fatty substance). It works as an emulsifier and surfactant to help mix oils and water-based ingredients together in the medicine.
  • UNII 059QF0KO0R
    Water is a liquid solvent that dissolves and mixes ingredients together in liquid medicines, syrups, and injections. It helps distribute the active drug evenly throughout the product.

6 inactive ingredients listed in the exact product block matched to this NDC.

The official label also statesbenzyl alcohol, light mineral oil, propylene glycol, purified water, sucrose distearate, sucrose stearate

Label-section wording can be broader than the structured product block and may mention additional formulation ingredients.

Where does this data come from?
Data sourced from official FDA Structured Product Labeling (SPL) via DailyMed — ingredient classCode="IACT" elements from the exact product block matched by this NDC. Label-section narrative from DailyMed / the openFDA label index is shown separately when available.

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

LabelerWalgreens
Application holderP AND L DEVELOPMENT LLC
FDA applicationANDA212385 (ANDA)
Labeler code00363
First marketedDec 2023
Product typeHuman Otc Drug
Portfolio342 products on file
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 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose 📄 Do Not Use 📄 When Using This Product 📄 Stop Use and Ask a Doctor If 📄 Keep Out of Reach of Children 📄 Questions or Comments 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 22 words ▾

Uses treats cold sores/fever blisters on the face or lips shortens healing time and duration of symptoms: tingling, pain, burning, and/or itching

⏱️ Dosage and Administration 58 words ▾

Directions adults and children 12 years or over: wash hands before and after applying cream apply to affected area on the face or lips at the first sign of cold sore/fever blister (tingle). early treatment ensures the best results rub in gently but completely use 5 times a day until healed children under 12 years: ask a doctor

⚠️ Warnings 37 words ▾

Warnings Allergy Alert: This product may cause a severe allergic reaction. Symptoms may include: hives facial swelling wheezing/difficulty shock rash If an allergic reaction occurs, stop use and seek medical help right away. For external use only

🧪 Active Ingredient 4 words ▾

Active ingredient Docosanol 10%

🧪 Inactive Ingredients 15 words ▾

Inactive ingredients benzyl alcohol, light mineral oil, propylene glycol, purified water, sucrose distearate, sucrose stearate

🎯 Purpose 5 words ▾

Purpose Cold sore/fever blister treatment

📄 Do Not Use 13 words ▾

Do not use if you are allergic to any ingredient in this product

📄 When Using This Product 36 words ▾

When using this product apply only to the affected areas do not use in or near the eyes avoid applying directly inside your mouth do not share this product with anyone. This may spread the infection.

📄 Stop Use and Ask a Doctor If 22 words ▾

Stop use and ask a doctor if your cold sore gets worse or the cold sore is not healed within 10 days

📄 Keep Out of Reach of Children 19 words ▾

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

📄 Questions or Comments 8 words ▾

Questions or comments? Call 1-877-753-3935 Monday-Friday 9AM-5PM EST

📄 Package Label / Principal Display Panel 97 words ▾

Principal Display Panel Compare to the active ingredient in Abreva®†† Docosanol Cream, 10% COLD SORE / FEVER BLISTER TREATMENT Only FDA approved medicine to shorten healing time* Cold sore treatment NET WT g (oz) ††This product is not manufactured or distributed by GlaxoSmithKline Consumer HealthcareHoldings (US) LLC, distributor of Abreva®. *Docosanol Cream, 10% contains the only OTC medicine approved by the FDA to shorten healing time and duration of symptoms. RETAIN THIS INSERT FOR FULL PRODUCT USES, DIRECTIONS AND WARNINGS DISTRIBUTED BY: WALGREEN CO.

DEERFIELD, IL 60015

Package Label WALGREENS Cold sore Fever Blister Treatment Docosanol 10%

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

About this NDC listing & data coverage

Over-the-counter (OTC) product
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

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 it is currently marketed — but Walgreens has reported a marketing end date of 2027-12-31, after which this package is expected to stop being marketed. The directory data on this page refreshes weekly.
Does this product come in other package sizes?
Yes — the FDA directory lists 1 other package presentation of this same product, including 2 tubes (00363-8980-14). Each has its own NDC and its own page — see the package list near the top of this page.
Who lists this product with the FDA?
Walgreens 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.
← 00363-8970-20 · Walgreens 00363-8989-12 · WALGREEN →
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.