Omeprazole
- Product NDC
- 55154-6648
- 11-digit product format
- 551546648
- Labeler code
- 55154
- Product ID
- 55154-6648_1d37d787-81ff-404e-a897-1bbdbeca7626
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Omeprazole
- Dosage form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Cardinal Health
- Application
- ANDA075576
- Marketing category
- ANDA
- Marketing start
- 2011-04-12
- Marketing end
- 2021-03-31
- 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
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55154-6648-0 | 55154664800 | 10 BLISTER PACK in 1 BAG (55154-6648-0) > 1 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK | 10 blister pack | 2011-04-12 | 2021-03-31 | No | No | Current |