Omeprazole
- Product NDC
- 71335-0559
- 11-digit product format
- 713350559
- Labeler code
- 71335
- Product ID
- 71335-0559_ab3965c2-13f2-4f73-829f-7506db229c1d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Omeprazole
- Dosage form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA075757
- Marketing category
- ANDA
- Marketing start
- 2003-01-28
- Marketing end
- 0000-00-00
- Substance
- OMEPRAZOLE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Cytochrome P450 2C19 Inhibitors [MoA], Proton Pump Inhibitor [EPC], Proton Pump Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71335-0559-1 | 71335055901 | 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0559-1) | 2018-02-16 | 0000-00-00 | No | No | Current |
| 71335-0559-2 | 71335055902 | 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0559-2) | 2018-03-02 | 0000-00-00 | No | No | Current |
| 71335-0559-3 | 71335055903 | 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0559-3) | 2021-12-27 | 0000-00-00 | No | No | Current |