PRILOSEC
- Product NDC
- 0186-0625
- 11-digit product format
- 001860625
- Labeler code
- 0186
- Product ID
- 0186-0625_3209e9cd-92a0-4e3d-8d26-cfb636faff9c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Omeprazole magnesium
- Dosage form
- GRANULE, DELAYED RELEASE
- Route
- ORAL
- Labeler
- AstraZeneca Pharmaceuticals LP
- Application
- NDA022056
- Marketing category
- NDA
- Marketing start
- 2002-02-09
- Marketing end
- 2019-11-01
- Substance
- OMEPRAZOLE MAGNESIUM
- Active strength
- 3 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