Omeprazole
- Product NDC
- 60760-395
- 11-digit product format
- 607600395
- Labeler code
- 60760
- Product ID
- 60760-395_960fca0c-f04b-6f90-e053-2995a90a74c0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- omeprazole
- Dosage form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Labeler
- St. Mary's Medical Park Pharmacy
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60760-395-30 | 60760039530 | 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (60760-395-30) | 2019-10-24 | 0000-00-00 | No | No | Current |