Omeprazole
- Product NDC
- 51660-029
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Omeprazole
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- OHM LABORATORIES INC.
- Application
- ANDA207891
- Marketing category
- ANDA
- Substance
- OMEPRAZOLE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 51660-029-14 | 1 BOTTLE in 1 CARTON (51660-029-14) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE | 2019-06-01 | | No | Historical |
| 51660-029-27 | 2 BOTTLE in 1 CARTON (51660-029-27) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE | 2019-06-01 | | No | Historical |
| 51660-029-44 | 3 BOTTLE in 1 CARTON (51660-029-44) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE | 2019-06-01 | | No | Historical |