omeprazole sodium bicarbonate
- Product NDC
- 71399-2440
- 11-digit product format
- 713992440
- Labeler code
- 71399
- Product ID
- 71399-2440_5295c2f0-e108-4ab4-be86-7947c1a6958c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- omeprazole sodium bicarbonate
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Akron Pharma Inc
- Application
- ANDA207476
- Marketing category
- ANDA
- Marketing start
- 2017-05-12
- 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
- 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 |
|---|
| 71399-2440-3 | 71399244003 | 30 CAPSULE in 1 BOTTLE (71399-2440-3) | 30 capsule | 2017-05-12 | 0000-00-00 | No | No | Current |