Omeprazole
- Product NDC
- 51660-061
- 11-digit product format
- 516600061
- Labeler code
- 51660
- Product ID
- 51660-061_0ae27ef3-b66f-469b-a0de-6cdd0a3a3a3f
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Omeprazole
- Dosage form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Ohm Laboratories Inc.
- Application
- ANDA210593
- Marketing category
- ANDA
- Marketing start
- 2018-07-21
- Marketing end
- 0000-00-00
- Substance
- OMEPRAZOLE MAGNESIUM
- Active strength
- 21 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 51660-061-14 | 51660006114 | 1 BOTTLE in 1 CARTON (51660-061-14) > 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE | 1 bottle | 2018-07-21 | 0000-00-00 | No | No | Current |
| 51660-061-27 | 51660006127 | 2 BOTTLE in 1 CARTON (51660-061-27) > 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE | 2 bottle | 2018-07-21 | 0000-00-00 | No | No | Current |
| 51660-061-44 | 51660006144 | 3 BOTTLE in 1 CARTON (51660-061-44) > 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE | 3 bottle | 2018-07-21 | 0000-00-00 | No | No | Current |