Omeprazole
- Product NDC
- 50436-3127
- 11-digit product format
- 504363127
- Labeler code
- 50436
- Product ID
- 50436-3127_fff53f05-b9b1-49e3-874f-df2dca0e19a7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Omeprazole
- Dosage form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Unit Dose Services
- Application
- ANDA076048
- Marketing category
- ANDA
- Marketing start
- 2003-11-11
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record