United States · FDA National Drug Code directory
Omeprazole
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
- 63548-7370_2cb02338-e348-4b60-aae0-e7806e03f5bf
- Product NDC
- 63548-7370
- Form
- TABLET, DELAYED RELEASE
- Composition / generic term
- Omeprazole
- Labeler
- PLD Acquisitions LLC DBA Avma Pharma Solutions
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20241031
- Source listing expiry
- 20271231
Source-listed ingredients
- OMEPRAZOLE MAGNESIUM — 20.6 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE, PLASTIC in 1 BOX (63548-7370-2) / 42 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC · 63548-7370-2
- 1 BOTTLE, PLASTIC in 1 BOX (63548-7370-4) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC · 63548-7370-4
- 1 BOTTLE, PLASTIC in 1 BOX (63548-7370-8) / 28 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC · 63548-7370-8
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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