United States · FDA National Drug Code directory
Amoxicillin
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 70518-2190_57208611-e892-2bd9-e063-6394a90a2bc4
- Product NDC
- 70518-2190
- Form
- CAPSULE
- Composition / generic term
- Amoxicillin
- Labeler
- REMEDYREPACK INC.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20190709
- Source listing expiry
- 20271231
Source-listed ingredients
- AMOXICILLIN — 500 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 28 CAPSULE in 1 BLISTER PACK (70518-2190-0) · 70518-2190-0
- 21 CAPSULE in 1 BLISTER PACK (70518-2190-1) · 70518-2190-1
- 30 CAPSULE in 1 BLISTER PACK (70518-2190-2) · 70518-2190-2
- 30 CAPSULE in 1 BOTTLE, PLASTIC (70518-2190-3) · 70518-2190-3
- 21 CAPSULE in 1 BOTTLE, PLASTIC (70518-2190-4) · 70518-2190-4
- 20 CAPSULE in 1 BOTTLE, PLASTIC (70518-2190-5) · 70518-2190-5
- 100 POUCH in 1 BOX (70518-2190-7) / 1 CAPSULE in 1 POUCH (70518-2190-6) · 70518-2190-7
- 14 CAPSULE in 1 BOTTLE, PLASTIC (70518-2190-8) · 70518-2190-8
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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