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
- 62756-377_676e2f39-d83e-485a-9366-ed14c382e466
- Product NDC
- 62756-377
- Form
- TABLET, DELAYED RELEASE
- Composition / generic term
- Omeprazole
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20190101
- Source listing expiry
- 20261231
Source-listed ingredients
- OMEPRAZOLE — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 2 BOTTLE in 1 CARTON (62756-377-11) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE · 62756-377-11
- 3 BOTTLE in 1 CARTON (62756-377-12) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE · 62756-377-12
- 1 BOTTLE in 1 CARTON (62756-377-21) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE · 62756-377-21
- 1 BLISTER PACK in 1 CARTON (62756-377-70) / 14 TABLET, DELAYED RELEASE in 1 BLISTER PACK · 62756-377-70
- 3 BLISTER PACK in 1 CARTON (62756-377-79) / 14 TABLET, DELAYED RELEASE in 1 BLISTER PACK · 62756-377-79
- 2 BLISTER PACK in 1 CARTON (62756-377-96) / 14 TABLET, DELAYED RELEASE in 1 BLISTER PACK · 62756-377-96
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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