United States · FDA National Drug Code directory
Acid Reducer
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
- 58602-729_81d45120-49d4-4de8-8477-79312e2c1d56
- Product NDC
- 58602-729
- Form
- TABLET, DELAYED RELEASE
- Composition / generic term
- Omeprazole
- Labeler
- Aurohealth LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20180606
- Source listing expiry
- 20261231
Source-listed ingredients
- OMEPRAZOLE MAGNESIUM — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BLISTER PACK in 1 CARTON (58602-729-01) / 14 TABLET, DELAYED RELEASE in 1 BLISTER PACK · 58602-729-01
- 2 BLISTER PACK in 1 CARTON (58602-729-02) / 14 TABLET, DELAYED RELEASE in 1 BLISTER PACK · 58602-729-02
- 3 BLISTER PACK in 1 CARTON (58602-729-03) / 14 TABLET, DELAYED RELEASE in 1 BLISTER PACK · 58602-729-03
- 1 BOTTLE in 1 CARTON (58602-729-05) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE · 58602-729-05
- 2 BOTTLE in 1 CARTON (58602-729-61) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE · 58602-729-61
- 3 BOTTLE in 1 CARTON (58602-729-62) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE · 58602-729-62
- 2 BLISTER PACK in 1 CARTON (58602-729-65) / 7 TABLET, DELAYED RELEASE in 1 BLISTER PACK (58602-729-64) · 58602-729-65
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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