Omeprazole/Sodium Bicarbonate
- Product NDC
- 49884-269
- 11-digit product format
- 498840269
- Labeler code
- 49884
- Product ID
- 49884-269_d01c3df2-2286-4a20-bbdb-939148dd30dd
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Omeprazole and Sodium Bicarbonate
- Dosage form
- POWDER, FOR SUSPENSION
- Route
- ORAL
- Labeler
- Par Pharmaceutical, Inc.
- Application
- ANDA079182
- Marketing category
- ANDA
- Marketing start
- 2016-07-18
- Marketing end
- 0000-00-00
- Substance
- OMEPRAZOLE; SODIUM BICARBONATE
- Active strength
- 40 mg/1; mg/1
- Pharmacologic classes
- Alkalinizing Activity [MoA], Cytochrome P450 2C19 Inhibitors [MoA], Proton Pump Inhibitor [EPC], Proton Pump Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 49884-269-11 | 49884026911 | 30 PACKET in 1 CARTON (49884-269-11) > 1 POWDER, FOR SUSPENSION in 1 PACKET (49884-269-52) | 30 packet | 2016-07-18 | 0000-00-00 | No | No | Current |