Omeprazole
- Product NDC
- 59726-737
- 11-digit product format
- 597260737
- Labeler code
- 59726
- Product ID
- 59726-737_934e98be-197e-48f3-829e-f46ad0bb90f2
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Omeprazole magnesium
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- P & L Development, LLC
- Application
- ANDA206582
- Marketing category
- ANDA
- Marketing start
- 2020-06-02
- Marketing end
- 0000-00-00
- Substance
- OMEPRAZOLE MAGNESIUM
- Active strength
- 21 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 59726-737 | OMEPRAZOLE (OMEPRAZOLE MAGNESIUM) TABLET, DELAYED RELEASE [P & L DEVELOPMENT, LLC] | 16 | Legacy NDC | 20230421_c9d30986-304a-408a-a48c-eee1ed0bf301.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 59726-737-14 | 59726073714 | 1 BOTTLE in 1 CARTON (59726-737-14) > 14 TABLET, DELAYED RELEASE in 1 BOTTLE | 1 bottle | 2020-06-02 | 0000-00-00 | No | No | Current |
| 59726-737-28 | 59726073728 | 2 BOTTLE in 1 CARTON (59726-737-28) > 14 TABLET, DELAYED RELEASE in 1 BOTTLE | 2 bottle | 2020-06-02 | 0000-00-00 | No | No | Current |
| 59726-737-42 | 59726073742 | 3 BOTTLE in 1 CARTON (59726-737-42) > 14 TABLET, DELAYED RELEASE in 1 BOTTLE | 3 bottle | 2020-06-02 | 0000-00-00 | No | No | Current |