omeprazole/sodium bicarbonate
- Product NDC
- 66993-412
- 11-digit product format
- 669930412
- Labeler code
- 66993
- Product ID
- 66993-412_091bd0ba-b3a9-4cfe-b680-ae8ff1f105e0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- omeprazole, sodium bicarbonate
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Prasco Laboratories
- Application
- NDA021849
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2006-02-27
- Marketing end
- 0000-00-00
- Substance
- OMEPRAZOLE; SODIUM BICARBONATE
- Active strength
- 20 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
- 2020-12-31
- 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 |
|---|
| 66993-412-30 | 66993041230 | 30 CAPSULE in 1 BOTTLE (66993-412-30) | 30 capsule | 2006-02-27 | 0000-00-00 | No | No | Current |