Benzonatate 100 mg Capsule, 30-count — NDC 70518-4558-0 (Billing 70518-4558-00)
by REMEDYREPACK INC. · 30 CAPSULE in 1 BOTTLE, PLASTIC
This is a package of 30 capsules of Benzonatate 100 mg Capsule from REMEDYREPACK INC., marketed since Feb 2026 and currently FDA-listed. It is the main listing for this product, which comes in 4 package sizes.
NDC 70518-4558-00
🏷️ FDA NDC (as labeled)
70518-4558-0
billing pads the package segment with a zero
This package
Contains30-count
Pack sizes4 compare ↓
Main listing for product 70518-4558 · Also comes in:
8 capsules 70518-4558-2
9 capsules 70518-4558-3
21 capsules 70518-4558-1
🗂️ FDA directory synced Oct 8, 2026 · this listing last changed Oct 8, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →
NDC database record
One package, one record: these facts belong to NDC 70518-4558-0 alone.
- Record
- FDA NDC Directory package listing · Human prescription drug
- Code segments
- 70518 labeler · 4558 product · 0 package
- Package marketed since
- Feb 1, 2026
- Sample package
- No — commercial package
- Listing certified through
- Dec 31, 2027
- Barcode (UPC-A, from the NDC)
- 3 7051845580 8
- FDA record last changed
- Oct 8, 2026
⚠️
Other active recalls for Benzonatate (different manufacturers) — 1 · tap to view
These affect other manufacturers’ products for the same ingredient — not necessarily the exact NDC on this page.
Class III · Dec 26, 2023 — Superpotent drug: Assay results were slightly above specification at the time zero point. (Amerisource Health Services LLC) · FDA recall D-0257-2024
Each entry is an official FDA enforcement report — look up any recall number in the FDA recall database ↗
Identity & classification
Regulatory identifiers FDA, NLM and CMS codes for this package
FDA NDC (as labeled)
70518-4558-0
Product NDC
70518-4558
11-digit billing NDC
70518455800
Application #
ANDA202765
SPL Set ID
5b9f0a5c-deec-ce69-e063-6294a90ac856
Established class (EPC)
Non-narcotic Antitussive
Physiologic effect
Decreased Tracheobronchial Stretch Receptor Activity
DEA schedule
Non-controlled
Marketing category
ANDA
Marketing status
On market
FDA listing status
Listed (active directory)
Marketing start
2026-02-01
Route
ORAL
Dosage form
CAPSULE
Substance
BENZONATATE
TE code (Orange Book)
AA · RLD · RS
Why two NDCs?
The FDA registers this code as 70518-4558-0 — a 5-4-1 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 package segment → 70518-4558-00. 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.
- FDA openFDA NDC Directory · synced Oct 8, 2026
- FDA label on DailyMed · label index refreshed Oct 6, 2026
- RxNorm (NLM RxNav) · catalog refreshed Oct 1, 2026
- Medi-Span GPI (licensed)
- First Databank (licensed) · refreshed Oct 8, 2026
Clinical
📖 What it is MedlinePlus · NLM
Benzonatate is used to relieve cough. Benzonatate is in a class of medications called antitussives (cough suppressants). It works by reducing the cough reflex in the lungs and air passages.
Read the full MedlinePlus article ↗📗 Our plain-language guide HelloPharmacist
- No, benzonatate is not related to codeine or narcotic cough medicines. Instead of working on your brain, it acts more like a local anesthetic inside your airways — it numbs the ner...
- What exactly does benzonatate do — is it like cough syrup with codeine?
- This is one of the most important things to know about benzonatate. The medicine inside acts like a numbing agent — if the capsule breaks open in your mouth, it can rapidly numb yo...
- Why does my pharmacist keep telling me not to chew the capsule?
Patient education
Supplement & herbal interactions
Some supplements/herbs that may interact with Benzonatate — tap one for details:
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.
- MedlinePlus (NLM) · refreshed Oct 1, 2026
- FDA label on DailyMed · label index refreshed Oct 6, 2026
💬 Questions about Benzonatate?
Ask a pharmacist →
Ask a licensed pharmacist directly — free, answered by our team.
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 system | Per each | Per 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.
- CMS NADAC weekly file
- CMS ASP pricing files · refreshed Sep 20, 2026
- CMS Medicaid State Drug Utilization Data · refreshed Oct 8, 2026
- CMS Part D plan pricing files · refreshed Sep 24, 2026
- VA National Acquisition Center price file
Packaging — all sizes for this product
| Package NDC | Description | Marketing start | Marketing end | Status |
|---|---|---|---|---|
| 70518-4558-00 You're viewing this Main listing | 30 CAPSULE in 1 BOTTLE, PLASTIC | 2026-02-01 | — | Active |
| 70518-4558-01 70518-4558-1 | 21 CAPSULE in 1 BOTTLE, PLASTIC | 2026-08-04 | — | Active |
| 70518-4558-02 70518-4558-2 | 8 CAPSULE in 1 BOTTLE, PLASTIC | 2026-08-25 | — | Active |
| 70518-4558-03 70518-4558-3 | 9 CAPSULE in 1 BOTTLE, PLASTIC | 2026-08-26 | — | Active |
You're viewing the largest of 4 pack sizes for this product.
Pack size FAQ
What quantity is in this package?
This is a 30-count package — 30 capsule in 1 bottle, plastic.
How does this package differ from NDC 70518-4558-02?
Both are Benzonatate 100 mg Capsule — the drug itself is identical. This page's package is the 30-count one, while NDC 70518-4558-02 is the 8 capsules package.
What NDC number is used to bill for this package of Benzonatate 100 mg Capsule?
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
| Product | Labeler | Pack | NADAC/unit | TE | Status | Price vs. this |
|---|---|---|---|---|---|---|
| Benzonatate 100 mg 00904-6564-60 | Major | 100 capsules | $0.066 | AA | Availability likely | — |
| Benzonatate 100 mg 00904-7153-61 | Major | 100 capsules | $0.066 | AA | Availability likely | — |
| Benzonatate 100 mg 23155-0898-01 | Heritage | 100 capsules | $0.066 | AA | Availability likely | — |
| Benzonatate 100 mg 31722-0956-01 | Camber | 100 capsules | $0.066 | AA | Availability likely | — |
| Benzonatate 100 mg 42806-0714-01 | Epic | 100 capsules | $0.066 | AA | Availability likely | — |
| Benzonatate 100 mg 49483-0946-01 | TIME | 100 capsules | $0.066 | AA | Availability likely | — |
| Benzonatate 100 mg 62135-0440-31 | Chartwell | 300 capsules | $0.066 | AA | Availability likely | — |
| Benzonatate 100 mg 64380-0712-06 | Strides | 100 capsules | $0.066 | AA | Availability likely | — |
| Benzonatate 100 mg 64980-0634-01 | Rising | 100 capsules | $0.066 | AA | Availability likely | — |
| Benzonatate 100 mg 67877-0573-01 | Ascend | 100 capsules | $0.066 | AA | Availability likely | — |
| Benzonatate 100 mg 68084-0214-01 | American | 100 capsules | $0.066 | AA | Availability likely | — |
| Benzonatate 100 mg 68382-0247-01 | Zydus | 100 capsules | $0.066 | AA | Availability likely | — |
| Benzonatate 100 mg 69452-0143-20 | Bionpharma | 100 capsules | $0.066 | AA | Availability likely | — |
| Benzonatate 100 mg 51224-0010-50 | TAGI | 100 capsules | $0.083 | AA | FDA listed | — |
| Benzonatate 100 mg 00615-8403-39 | NCS | 30 capsules | — | AA | FDA listed | — |
| Benzonatate 100 mg 25000-0002-03 | MARKSANS | 30 capsules | — | AA | FDA listed | — |
| Benzonatate 100 mg 42291-0091-01 | AvKARE | 100 capsules | — | AA | FDA listed | — |
| Benzonatate 100 mg 50090-4968-00 | A-S | 15 capsules | — | AA | FDA listed | — |
| Benzonatate 100 mg 50090-4969-00 | A-S | 20 capsules | — | AA | FDA listed | — |
| Benzonatate 100 mg 50090-5409-00 | A-S | 20 capsules | — | AA | FDA listed | — |
| Benzonatate 100 mg 50090-5986-00 | A-S | 15 capsules | — | AA | FDA listed | — |
| Benzonatate 100 mg 50090-6387-00 | A-S | 20 capsules | — | AA | FDA listed | — |
| Benzonatate 100 mg 50090-6850-00 | A-S | 15 capsules | — | AA | FDA listed | — |
| Benzonatate 100 mg 51655-0754-20 | Northwind | 20 capsules | — | AA | FDA listed | — |
| Benzonatate 100 mg 55154-3372-00 | Cardinal | 10 capsules | — | AA | FDA listed | — |
| Benzonatate 100 mg 60429-0927-01 | Golden | 100 capsules | — | AA | FDA listed | — |
| Benzonatate 100 mg 60760-0700-30 | St. | 30 capsules | — | AA | FDA listed | — |
| Benzonatate 100 mg 60760-0869-15 | St. | 15 capsules | — | AA | FDA listed | — |
| Benzonatate 100 mg 61919-0400-20 | DIRECT | 20 capsules | — | AA | FDA listed | — |
| Benzonatate 100 mg 63187-0076-14 | Proficient | 14 capsules | — | AA | FDA listed | — |
| Benzonatate 100 mg 63187-0799-14 | Proficient | 14 capsules | — | AA | FDA listed | — |
| benzonatate 100 mg 63187-0928-10 | Proficient | 10 capsules | — | AA | FDA listed | — |
| Benzonatate 100 mg 63629-2473-01 | Bryant | 500 capsules | — | AA | FDA listed | — |
| Benzonatate 100 mg 63629-2474-01 | Bryant | 100 capsules | — | AA | FDA listed | — |
| Benzonatate 100 mg 63629-9189-01 | Bryant | 500 capsules | — | AA | FDA listed | — |
| Benzonatate 100 mg 65162-0536-10 | Amneal | 100 capsules | — | AA | FDA listed | — |
| Benzonatate 100 mg 65841-0614-01 | Zydus | 100 capsules | — | AA | FDA listed | — |
| Benzonatate 100 mg 67046-1484-03 | Coupler | 30 capsules | — | AA | FDA listed | — |
| Benzonatate 100 mg 67046-1629-03 | Coupler | 30 capsules | — | AA | FDA listed | — |
| Benzonatate 100 mg 67296-2194-01 | Redpharm | 15 capsules | — | AA | FDA listed | — |
| Benzonatate 100 mg 67296-2207-01 | Redpharm | 15 capsules | — | AA | FDA listed | — |
| Benzonatate 100 mg 68071-5083-03 | NuCare | 30 capsules | — | AA | FDA listed | — |
| Benzonatate 100 mg 68071-5105-04 | NuCare | 4 capsules | — | AA | FDA listed | — |
| Benzonatate 100 mg 68071-5156-02 | NuCare | 20 capsules | — | AA | FDA listed | — |
| Benzonatate 100 mg 68071-5223-04 | NuCare | 4 capsules | — | AA | FDA listed | — |
| Benzonatate 100 mg 68094-0798-50 | Precision | 100 capsules | — | AA | FDA listed | — |
| Benzonatate 100 mg 68788-7607-00 | Preferred | 9 capsules | — | AA | FDA listed | — |
| Benzonatate 100 mg 70518-2873-00 | REMEDYREPACK | 10 capsules | — | AA | FDA listed | — |
| Benzonatate 100 mgthis 70518-4558-00 | REMEDYREPACK | 30 capsules | — | AA | FDA listed | — |
| Benzonatate 100 mg 71205-0067-10 | Proficient | 10 capsules | — | AA | FDA listed | — |
| Benzonatate 100 mg 71205-0632-10 | Proficient | 10 capsules | — | AA | FDA listed | — |
| Benzonatate 100 mg 71205-0699-10 | Proficient | 10 capsules | — | AA | FDA listed | — |
| Benzonatate 100 mg 71205-0853-00 | Proficient | 100 capsules | — | AA | FDA listed | — |
| benzonatate 100 mg 71205-0971-00 | Proficient | 100 capsules | — | AA | FDA listed | — |
| Benzonatate 100 mg 71335-0091-00 | Bryant | 10 capsules | — | AA | FDA listed | — |
| benzonatate 100 mg 71335-0688-00 | Bryant | 10 capsules | — | AA | FDA listed | — |
| benzonatate 100 mg 71335-1329-00 | Bryant | 10 capsules | — | AA | FDA listed | — |
| Benzonatate 100 mg 71335-1544-00 | Bryant | 10 capsules | — | AA | FDA listed | — |
| Benzonatate 100 mg 71335-1927-00 | Bryant | 10 capsules | — | AA | FDA listed | — |
| Benzonatate 100 mg 71335-1968-00 | Bryant | 10 capsules | — | AA | FDA listed | — |
| Benzonatate 100 mg 71335-2672-01 | Bryant | 500 capsules | — | AA | FDA listed | — |
| Benzonatate 100 mg 71335-3068-00 | Bryant | 10 capsules | — | AA | FDA listed | — |
| Benzonatate 100 mg 71610-0692-30 | Aphena | 30 capsules | — | AA | FDA listed | — |
| Benzonatate 100 mg 72162-1561-01 | Bryant | 100 capsules | — | AA | FDA listed | — |
| Benzonatate 100 mg 72189-0194-20 | DIRECT | 20 capsules | — | AA | FDA listed | — |
| Benzonatate 100 mg 72789-0230-06 | PD-Rx | 6 capsules | — | AA | FDA listed | — |
| Benzonatate 100 mg 72789-0231-15 | PD-Rx | 15 capsules | — | AA | FDA listed | — |
| Benzonatate 100 mg 72865-0117-01 | XLCare | 100 capsules | — | AA | FDA listed | — |
| Benzonatate 100 mg 76420-0803-01 | Asclemed | 100 capsules | — | AA | FDA listed | — |
| Benzonatate 100 mg 85766-0066-01 | Sportpharm | 100 capsules | — | AA | FDA listed | — |
| Benzonatate 100 mg 85766-0089-01 | Sportpharm | 100 capsules | — | AA | FDA listed | — |
| Benzonatate 100 mg 00615-8661-05 | NCS | 15 capsules | — | AA | 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.
- FDA openFDA NDC Directory · synced Oct 8, 2026
- FDA Orange Book · refreshed Oct 3, 2026
- CMS NADAC weekly file
Availability & generic status
🏛️
2026
On the market since
Feb 2026
📍
2026
Currently FDA-listed
listed with the FDA
🔓
·
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.
- FDA Orange Book · refreshed Oct 3, 2026
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.
🧪 Avoiding an ingredient? See Benzonatate inactive ingredients by manufacturer: every current product's list side by side, so you can ask your pharmacy for the version that does not list it.
Loading inactive ingredients from the official FDA label in the background. No external source is being called by this page request.
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.- FDA label on DailyMed · label index refreshed Oct 6, 2026
- FDA openFDA NDC Directory · synced Oct 8, 2026
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
LabelerREMEDYREPACK INC.
Application holderCSPC-NBP PHARMACEUTICAL CO LTD
FDA applicationANDA202765 (ANDA)
Labeler code70518
First marketedFeb 2026
Product typeHuman Prescription Drug
Portfolio1,529 products on file
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- divalproex sodium 500 mg Tablet, Film Coated, Extended Release NDC 70518-4553-0
- Trifluoperazine Hydrochloride 2 mg Tablet, Film Coated NDC 70518-4554-0
- Dicyclomine hydrochloride 20 mg Tablet NDC 70518-4555-0
- Allopurinol 300 mg Tablet NDC 70518-4556-0
- divalproex sodium 250 mg Tablet, Film Coated, Extended Release NDC 70518-4557-0
- Metaxalone 800 mg Tablet NDC 70518-4559-0
- Prednisone 10 mg Tablet NDC 70518-4560-0
- Lacosamide 100 mg Tablet, Film Coated NDC 70518-4561-0
- Lacosamide 100 mg Tablet, Film Coated NDC 70518-4562-0
- Lurasidone Hydrochloride 20 mg Tablet, Film Coated NDC 70518-4563-0
- Guanfacine Gaunfacine 2 mg Tablet NDC 70518-4564-0
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 openFDA NDC Directory · synced Oct 8, 2026
- Drugs@FDA
Full prescribing information FDA SPL
The complete FDA label for this product — the official prescribing information, verbatim, section by section. Jump with a chip, search within the label, or expand everything.
📄 FDA label ▾
No FDA label is on file for this product yet. Labels load from openFDA / DailyMed and refresh weekly.
No label section mentions that — try another word, or open the full label on DailyMed below.
Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA.
Prefer the government’s original formatting? View this label on DailyMed ↗
Medicare Part D spend CMS · PART D · 2026 (Q1)
Medicare Part D (outpatient prescription) spending for Benzonatate — the program that covers self-administered drugs. 12 manufacturers.
⚠️ Drug-level data: CMS publishes Part D spending by drug, not by NDC — these figures combine every manufacturer, strength and package size sold under the name Benzonatate. That’s a different level of aggregation than the Medicaid card above, which is specific to this exact 11-digit NDC (pack size included), so the two aren’t directly comparable.
Period
Total Part D spend
$654.6K
Claims incl. refills
49.4K
Beneficiaries
42.4K
Spend / beneficiary
$15.42
Spend / claim
$13.25
Trend by period
💵 About the dollar figures: spending is what Part D plans paid before confidential manufacturer rebates, so the program’s real net cost is lower. A blank patient count means fewer than 11 people — CMS hides counts that small to protect privacy. Source: CMS Medicare Quarterly Part D Spending by Drug (data.cms.gov), updated quarterly.
About this NDC listing & data coverage
Finished prescription 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 | — Not published for this NDC No photo available yet for this listing. |
| Inactive ingredients (structured) | — Not published for this NDC The labeler did not submit a structured excipient list, or no SPL is 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 | ✓ Available |
| 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: this package is listed as actively marketed, with no marketing end date reported by REMEDYREPACK INC.. Listing status can change — the directory data on this page refreshes weekly.
Does this product come in other package sizes?
Yes — the FDA directory lists 3 other package presentations of this same product, including 8 capsules (70518-4558-02), 9 capsules (70518-4558-03), 21 capsules (70518-4558-01). 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?
REMEDYREPACK 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 a prescription product, so it is dispensed under a prescriber's order. Your pharmacist can tell you whether any over-the-counter forms of the same medication exist.
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.
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.