Omeprazole
- Product NDC
- 68071-4140
- 11-digit product format
- 680714140
- Labeler code
- 68071
- Product ID
- 68071-4140_bb2d055f-25f7-3497-e053-2995a90a4457
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- omeprazole
- Dosage form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA075410
- Marketing category
- ANDA
- Marketing start
- 2009-01-23
- Marketing end
- 0000-00-00
- Substance
- OMEPRAZOLE
- Active strength
- 40 mg/1
- Pharmacologic classes
- Proton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA],Cytochrome P450 2C19 Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 68071-4140-3 | 68071414003 | 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68071-4140-3) | 2017-10-31 | 0000-00-00 | No | No | Current |