Omeprazole and Sodium Bicarbonate
- Product NDC
- 16714-509
- 11-digit product format
- 167140509
- Labeler code
- 16714
- Product ID
- 16714-509_bb92ad91-4099-4507-bb54-0ccfb0fe5849
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Omeprazole and Sodium Bicarbonate
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Northstar Rx LLC
- Application
- ANDA204228
- Marketing category
- ANDA
- Marketing start
- 2016-07-15
- Marketing end
- 0000-00-00
- Substance
- OMEPRAZOLE; SODIUM BICARBONATE
- Active strength
- 40 mg/1; mg/1
- Pharmacologic classes
- Proton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA],Cytochrome P450 2C19 Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record