Esomeprazole Magnesium
- Product NDC
- 68071-5074
- 11-digit product format
- 680715074
- Labeler code
- 68071
- Product ID
- 68071-5074_bbb7a0c8-3889-5eb0-e053-2995a90aa8ec
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Esomeprazole Magnesium
- Dosage form
- CAPSULE, DELAYED RELEASE PELLETS
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA205563
- Marketing category
- ANDA
- Marketing start
- 2017-09-01
- Marketing end
- 0000-00-00
- Substance
- ESOMEPRAZOLE MAGNESIUM
- Active strength
- 20 mg/1
- Pharmacologic classes
- Proton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA],Cytochrome P450 2C19 Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-5074-6 | 68071507406 | 60 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (68071-5074-6) | 2019-09-30 | 0000-00-00 | No | No | Current |