Home › NDC Lookup › Ingredients › Amoxicillin And Clavulanate Potassium › 70518-4758-00
Amoxicillin and Clavulanate Potassium 875 mg; 125 mg Tablet, Coated — NDC 70518-4758-00 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Amoxicillin and Clavulanate Potassium 875 mg; 125 mg Tablet, Coated — NDC 70518-4758-0 (Billing 70518-4758-00)

by REMEDYREPACK INC. · 100 POUCH in 1 BOX / 1 TABLET, COATED in 1 POUCH

This is a package of Amoxicillin and Clavulanate Potassium 875 mg; 125 mg Tablet, Coated from REMEDYREPACK INC., marketed since Sep 2026 and currently FDA-listed. It is this product's only package size.

NDC 70518-4758-00
🏷️ FDA NDC (as labeled) 70518-4758-0 billing pads the package segment with a zero
Rx only Brand On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 1, 2026 · this listing last changed Oct 2, 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) 70518-4758-0
Product NDC 70518-4758
11-digit billing NDC 70518475800
Application # NDA050720
SPL Set ID 2c857fb6-9c7d-4192-9f28-38d8dd57508b
Established class (EPC) Penicillin-class Antibacterial; beta Lactamase Inhibitor
Mechanism of action beta Lactamase Inhibitors
Chemical class Penicillins
DEA schedule Non-controlled
Marketing category NDA AUTHORIZED GENERIC
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2026-09-21
Route ORAL
Dosage form TABLET, COATED
Substance AMOXICILLIN; CLAVULANATE POTASSIUM
TE code (Orange Book) AB · RLD · RS
Why two NDCs? The FDA registers this code as 70518-4758-0 — 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 → 70518-4758-00. 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.

Clinical

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
70518-4758-00 You're viewing this Main listing 100 POUCH in 1 BOX / 1 TABLET, COATED in 1 POUCH 2026-09-21 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Amoxicillin and Clavulanate Potassium 875 mg/1; 125 mg 65862-0503-01 Aurobindo 100 tablets $0.284 AB Availability likely —
Amoxicillin and Clavulanate Potassium 875 mg/1; 125 mg 00093-2275-34 Teva 20 tablets $0.284 AB Availability likely —
Amoxicillin and Clavulanate Potassium 875 mg/1; 125 mg 00143-9249-20 Hikma 20 tablets $0.284 AB Availability likely —
Amoxicillin And Clavulanate Potassium 875 mg/1; 125 mg 42571-0162-01 Micro 100 tablets $0.284 AB Availability likely —
Amoxicillin and Clavulanate Potassium 875 mg/1; 125 mg 60687-0803-01 American 1 tablet $0.284 AB Availability likely —
Amoxicillin And Clavulanate Potassium 875 mg/1; 125 mg 81964-0221-14 USAntibiotics, 20 tablets $0.284 AB Availability likely —
Amoxicillin and Clavulanate Potassium 875 mg/1; 125 mg 00781-1852-01 Sandoz 100 tablets $0.284 AB Availability likely —
Amoxicillin and Clavulanate Potassium 875 mg/1; 125 mg 16714-0297-01 NorthStar 20 tablets $0.284 AB Availability likely —
Amoxicillin and Clavulanate Potassium 875 mg/1; 125 mg 16714-0014-01 Northstar 20 tablets $0.340 AB Discontinued —
Amoxicillin and Clavulanate Potassium 875 mg/1; 125 mg 63187-0014-14 Proficient 14 tablets — AB FDA listed —
Amoxicillin and Clavulanate Potassium 875 mg/1; 125 mg 63187-0488-14 Proficient 14 tablets — AB FDA listed —
Amoxicillin And Clavulanate Potassium 875 mg/1; 125 mg 71205-0331-14 Proficient 14 tablets — AB FDA listed —
Amoxicillin and Clavulanate Potassium 875 mg/1; 125 mg 71205-0651-10 Proficient 10 tablets — AB FDA listed —
Amoxicillin And Clavulanate Potassium 875 mg/1; 125 mg 76420-0005-20 Asclemed 20 tablets — AB FDA listed —
Amoxicillin and Clavulanate Potassium 875 mg/1; 125 mg 71205-0712-10 Proficient 10 tablets — AB FDA listed —
Amoxicillin and Clavulanate Potassium 875 mg/1; 125 mg 76420-0529-20 Asclemed 20 tablets — AB FDA listed —
Amoxicillin and Clavulanate Potassium 875 mg/1; 125 mg 76420-0607-01 Asclemed 100 tablets — AB FDA listed —
Amoxicillin and Clavulanate Potassium 875 mg/1; 125 mg 68071-2982-02 NuCare 20 tablets — AB FDA listed —
Amoxicillin and Clavulanate Potassium 875 mg/1; 125 mg 68071-3842-02 NuCare 20 tablets — AB FDA listed —
Amoxicillin and Clavulanate Potassium 875 mg/1; 125 mg 68071-3866-03 NuCare 30 tablets — AB FDA listed —
Amoxicillin And Clavulanate Potassium 875 mg/1; 125 mg 70518-2263-03 REMEDYREPACK 1 tablet — AB FDA listed —
Amoxicillin and Clavulanate Potassium 875 mg/1; 125 mg 70518-3604-00 REMEDYREPACK 1 tablet — AB Discontinued —
Amoxicillin and Clavulanate Potassium 875 mg/1; 125 mg 70518-3624-00 REMEDYREPACK 1 tablet — AB Discontinued —
Amoxicillin And Clavulanate Potassium 875 mg/1; 125 mg 85766-0171-14 Sportpharm 14 tablets — AB FDA listed —
Amoxicillin and Clavulanate Potassium 875 mg/1; 125 mg 67046-0955-03 Coupler 30 tablets — AB FDA listed —
Amoxicillin And Clavulanate Potassium 875 mg/1; 125 mg 68788-8307-02 Preferred 20 tablets — AB FDA listed —
Amoxicillin and Clavulanate Potassium 875 mg/1; 125 mg 76420-0501-20 Asclemed 20 tablets — AB FDA listed —
Amoxicillin And Clavulanate Potassium 875 mg/1; 125 mg 82804-0060-20 Proficient 20 tablets — AB FDA listed —
Amoxicillin and Clavulanate Potassium 875 mg/1; 125 mg 82804-0177-14 Proficient 14 tablets — AB FDA listed —
Amoxicillin and Clavulanate Potassium 875 mg/1; 125 mg 50090-1809-00 A-S 20 tablets — AB FDA listed —
Amoxicillin And Clavulanate Potassium 875 mg/1; 125 mg 50090-6324-00 A-S 20 tablets — AB FDA listed —
Amoxicillin and Clavulanate Potassium 875 mg/1; 125 mg 68071-3860-02 NuCare 20 tablets — AB FDA listed —
Amoxicillin and Clavulanate Potassium 875 mg/1; 125 mg 68071-3864-04 NuCare 14 tablets — AB FDA listed —
Amoxicillin and Clavulanate Potassium 875 mg/1; 125 mg 68071-4967-02 NuCare 20 tablets — AB FDA listed —
Amoxicillin and Clavulanate Potassium 875 mg/1; 125 mg 72789-0253-20 PD-Rx 20 tablets — AB FDA listed —
Amoxicillin and Clavulanate Potassium 875 mg/1; 125 mg 43063-0077-03 PD-Rx 3 tablets — AB FDA listed —
Amoxicillin and Clavulanate Potassium 875 mg/1; 125 mg 50090-3179-00 A-S 20 tablets — AB FDA listed —
Amoxicillin and Clavulanate Potassium 875 mg/1; 125 mg 50090-4413-00 A-S 20 tablets — AB FDA listed —
Amoxicillin and Clavulanate Potassium 875 mg/1; 125 mg 55289-0767-10 PD-Rx 10 tablets — AB FDA listed —
Amoxicillin And Clavulanate Potassium 875 mg/1; 125 mg 68071-4224-02 NuCare 20 tablets — AB FDA listed —
Amoxicillin and Clavulanate Potassium 875 mg/1; 125 mg 68071-4586-03 NuCare 30 tablets — AB FDA listed —
Amoxicillin and Clavulanate Potassium 875 mg/1; 125 mg 68071-5295-03 NuCare 3 tablets — AB FDA listed —
Amoxicillin and Clavulanate Potassium 875 mg/1; 125 mg 70518-2225-00 REMEDYREPACK 20 tablets — AB FDA listed —
Amoxicillin And Clavulanate Potassium 875 mg/1; 125 mg 70518-3967-00 REMEDYREPACK 28 tablets — AB Discontinued —
Amoxicillin and Clavulanate Potassium 875 mg/1; 125 mg 72162-2211-02 Bryant 20 tablets — AB FDA listed —
Amoxicillin and Clavulanate Potassium 875 mg/1; 125 mg 72789-0147-03 PD-Rx 3 tablets — AB FDA listed —
Amoxicillin and Clavulanate Potassium 875 mg/1; 125 mg 72789-0421-14 PD-Rx 14 tablets — AB FDA listed —
Amoxicillin and Clavulanate Potassium 875 mg/1; 125 mg 72789-0456-14 PD-Rx 14 tablets — AB FDA listed —
Amoxicillin and Clavulanate Potassium 875 mg/1; 125 mg 85766-0078-01 Sportpharm 100 tablets — AB FDA listed —
Amoxicillin and Clavulanate Potassium 875 mg/1; 125 mg 63629-4541-01 Bryant 14 tablets — AB FDA listed —
Amoxicillin And Clavulanate Potassium 875 mg/1; 125 mg 68071-3402-03 NuCare 30 tablets — AB FDA listed —
Amoxicillin and Clavulanate Potassium 875 mg/1; 125 mg 68071-5057-03 NuCare 3 tablets — AB FDA listed —
Amoxicillin and Clavulanate Potassium 875 mg/1; 125 mg 70518-4148-00 REMEDYREPACK 100 tablets — AB FDA listed —
Amoxicillin and Clavulanate Potassium 875 mg/1; 125 mg 71335-2787-01 Bryant 10 tablets — AB FDA listed —
Amoxicillin and Clavulanate Potassium 875 mg/1; 125 mg 71335-3138-01 Bryant 20 tablets — AB FDA listed —
Amoxicillin and Clavulanate Potassium 875 mg/1; 125 mg 73043-0006-20 Devatis, 20 tablets — AB FDA listed —
Amoxicillin And Clavulanate Potassium 875 mg/1; 125 mg 81964-0575-83 USAntibiotics, 180 tablets — AB Discontinued —
Amoxicillin and Clavulanate Potassium 875 mg/1; 125 mg 82804-0201-20 Proficient 20 tablets — AB FDA listed —
Amoxicillin and Clavulanate Potassium 875 mg/1; 125 mg 82868-0067-14 Northwind 14 tablets — AB FDA listed —
Amoxicillin And Clavulanate Potassium 875 mg/1; 125 mg 68788-7531-02 Preferred 20 tablets — AB FDA listed —
Amoxicillin and Clavulanate Potassium 875 mg/1; 125 mg 70518-4424-00 REMEDYREPACK 30 tablets — AB FDA listed —
Amoxicillin and Clavulanate Potassium 875 mg/1; 125 mg 80425-0279-01 Advanced 20 tablets — AB FDA listed —
Amoxicillin and Clavulanate Potassium 875 mg/1; 125 mg 43063-0377-02 PD-Rx 2 tablets — AB FDA listed —
Amoxicillin and Clavulanate Potassium 875 mg/1; 125 mg 50090-7003-00 A-S 14 tablets — AB FDA listed —
Amoxicillin and Clavulanate Potassium 875 mg/1; 125 mg 50090-7415-00 A-S 14 tablets — AB FDA listed —
Amoxicillin and Clavulanate Potassium 875 mg/1; 125 mg 68071-3822-03 NuCare 3 tablets — AB FDA listed —
Amoxicillin and Clavulanate Potassium 875 mg/1; 125 mg 68071-5065-03 NuCare 3 tablets — AB FDA listed —
Amoxicillin and Clavulanate Potassium 875 mg/1; 125 mg 85766-0019-01 Sportpharm 100 tablets — AB FDA listed —
Amoxicillin and Clavulanate Potassium 875 mg/1; 125 mg 50090-0822-00 A-S 20 tablets — AB FDA listed —
Amoxicillin And Clavulanate Potassium 875 mg/1; 125 mg 68071-4549-03 NuCare 3 tablets — AB FDA listed —
Amoxicillin And Clavulanate Potassium 875 mg/1; 125 mg 82868-0002-10 Northwind 10 tablets — AB FDA listed —
Amoxicillin and Clavulanate Potassium 875 mg/1; 125 mg 63187-0327-20 Proficient 20 tablets — AB FDA listed —
Amoxicillin and Clavulanate Potassium 875 mg/1; 125 mg 63629-5847-01 Bryant 6 tablets — AB FDA listed —
Amoxicillin and Clavulanate Potassium 875 mg/1; 125 mg 68071-5026-04 NuCare 14 tablets — AB FDA listed —
Amoxicillin And Clavulanate Potassium 875 mg/1; 125 mg 71335-2917-01 Bryant 100 tablets — AB FDA listed —
Amoxicillin and Clavulanate Potassium 875 mg/1; 125 mg 72789-0459-14 PD-Rx 14 tablets — AB FDA listed —
Amoxicillin And Clavulanate Potassium 875 mg/1; 125 mg 45865-0227-20 Medsource 20 tablets — AB FDA listed —
Amoxicillin and Clavulanate Potassium 875 mg/1; 125 mg 68788-8836-02 Preferred 20 tablets — AB FDA listed —
Amoxicillin and Clavulanate Potassium 875 mg/1; 125 mg 70518-3676-00 REMEDYREPACK 1 tablet — AB Discontinued —
Amoxicillin And Clavulanate Potassium 875 mg/1; 125 mg 72162-2434-01 Bryant 100 tablets — AB FDA listed —
Amoxicillin and Clavulanate Potassium 875 mg/1; 125 mg 68071-2751-02 NuCare 20 tablets — AB FDA listed —
Amoxicillin and Clavulanate Potassium 875 mg/1; 125 mg 68788-4158-02 Preferred 20 tablets — AB FDA listed —
amoxicillin and clavulanate potassium 875 mg/1; 125 mg 62135-0092-20 Chartwell 20 tablets — AB FDA listed —
Amoxicillin and Clavulanate Potassium 875 mg/1; 125 mg 72789-0585-28 PD-Rx 28 tablets — AB FDA listed —
Amoxicillin and Clavulanate Potassium 875 mg/1; 125 mg 85766-0268-01 Sportpharm 1 tablet — AB FDA listed —
Amoxicillin And Clavulanate Potassium 875 mg/1; 125 mgthis 70518-4758-00 REMEDYREPACK 1 tablet — AB FDA listed —
About this product: this is an authorized generic — the brand-name product marketed without its brand name. 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

🏛️
2026
On the market since
Sep 2026
📍
2026
Currently FDA-listed
listed with the FDA
🔓
·
Generic versions listed
see equivalents
✅Generic appears available

FDA-approved generic versions are listed, and recent pricing/market data suggests they may be available — see Therapeutic equivalents.

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
ShapeCapsule
ImprintAUGMENTIN;875
Size18 mm
ScoringScored — splits in 2
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 3NXW29V3WO
    Hypromellose is a plant-based thickener made from cellulose. It's used in medicines as a binder to hold ingredients together, a coating for tablets, and a thickener for liquids.
  • UNII 70097M6I30
    Magnesium stearate is a salt made from magnesium and stearic acid, a fatty substance. It's used in tablets and capsules as a lubricant and glidant to help ingredients flow smoothly during manufacturing and prevent sticking.
  • UNII OP1R32D61U
    Microcrystalline cellulose is a purified form of cellulose, a natural fiber from plant sources. It acts as a binder and filler in tablets and capsules, helping hold ingredients together and give the medicine its shape and size.
  • UNII 3WJQ0SDW1A
    Polyethylene glycol is a synthetic liquid or solid polymer used in medicines as a solvent, lubricant, and humectant. It helps dissolve active ingredients, reduces friction during manufacturing, and retains moisture in the final product.
  • UNII ETJ7Z6XBU4
    Silicon dioxide is a naturally occurring mineral used as a glidant and anti-caking agent. It helps powder ingredients flow smoothly and prevents clumping during manufacturing and storage.
  • UNII 5856J3G2A2
    A starch-based powder made from potatoes and processed with sodium. It acts as a disintegrant, helping the tablet or capsule break apart quickly in the stomach so the medicine can be absorbed.
  • UNII 15FIX9V2JP
    Titanium dioxide is a bright white mineral powder commonly used as a colorant and opacifying agent. It makes pills and tablets white or lighter in color and helps make coatings non-transparent.

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

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

LabelerREMEDYREPACK INC.
Application holderUS ANTIBIOTICS LLC
FDA applicationNDA050720 (NDA AUTHORIZED GENERIC)
Labeler code70518
First marketedSep 2026
Product typeHuman Prescription Drug
Portfolio1,527 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.

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
📄 FDA label 19 words ▾

No FDA label is on file for this product yet. Labels load from openFDA / DailyMed and refresh weekly.

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

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 ✓ 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 ✓ 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.
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.
← 70518-4757-00 · REMEDYREPACK 70518-4759-00 · REMEDYREPACK →
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.