Omeprazole
- Product NDC
- 21130-991
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Omeprazole
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Living Better Brands LLC
- Application
- ANDA207891
- Marketing category
- ANDA
- Substance
- OMEPRAZOLE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 21130-991-28 | 2 BLISTER PACK in 1 CARTON (21130-991-28) / 14 TABLET, DELAYED RELEASE in 1 BLISTER PACK | 2019-06-01 | | No | Historical |
| 21130-991-44 | 1 BLISTER PACK in 1 CARTON (21130-991-44) / 14 TABLET, DELAYED RELEASE in 1 BLISTER PACK | 2019-06-01 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Omeprazole | Living Better Brands LLC | Sun Pharmaceutical Industries Limited | 2024-08-12 | HUMAN OTC DRUG LABEL | 1 |