Omeprazole
- Product NDC
- 60760-521
- 11-digit product format
- 607600521
- Labeler code
- 60760
- Product ID
- 60760-521_7ad02cc4-7a56-7f0d-e053-2991aa0a4953
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Omeprazole
- Dosage form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Labeler
- St. Mary's Medical Park Pharmacy
- Application
- ANDA076048
- Marketing category
- ANDA
- Marketing start
- 2014-01-30
- Marketing end
- 0000-00-00
- Substance
- OMEPRAZOLE
- Active strength
- 20 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 |
|---|
| 60760-521-05 | 60760052105 | 5 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (60760-521-05) | 2014-03-17 | 0000-00-00 | No | No | Current |
| 60760-521-20 | 60760052120 | 20 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (60760-521-20) | 2018-02-15 | 0000-00-00 | No | No | Current |
| 60760-521-30 | 60760052130 | 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (60760-521-30) | 2014-02-21 | 0000-00-00 | No | No | Current |
| 60760-521-60 | 60760052160 | 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (60760-521-60) | 2014-10-10 | 0000-00-00 | No | No | Current |
| 60760-521-90 | 60760052190 | 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (60760-521-90) | 2014-01-30 | 0000-00-00 | No | No | Current |