United States · FDA National Drug Code directory
care one 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
- 41520-915_5248b065-e6de-4bc6-af17-ee5e7ecdc45f
- Product NDC
- 41520-915
- Form
- TABLET, DELAYED RELEASE
- Composition / generic term
- Omeprazole
- Labeler
- American Sales Company
- Marketing category
- NDA
- Marketing start / end (source format)
- 20080229
- Source listing expiry
- 20271231
Source-listed ingredients
- OMEPRAZOLE — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 3 BOTTLE in 1 CARTON (41520-915-03) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE · 41520-915-03
- 3 CARTON in 1 CARTON (41520-915-55) / 14 BLISTER PACK in 1 CARTON / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK · 41520-915-55
- 14 BLISTER PACK in 1 CARTON (41520-915-74) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK · 41520-915-74
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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