Esomeprazole Magnesium
- Product NDC
- 60687-235
- 11-digit product format
- 606870235
- Labeler code
- 60687
- Product ID
- 60687-235_7d7759e5-8d94-dc9a-e053-2991aa0a6484
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Esomeprazole Magnesium
- Dosage form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Labeler
- American Health Packaging
- Application
- ANDA078279
- Marketing category
- ANDA
- Marketing start
- 2017-03-22
- Marketing end
- 2019-03-31
- Substance
- ESOMEPRAZOLE MA
- Active strength
- 20 mg/1
- Pharmacologic classes
- Proton Pump Inh
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| R6DXU4WAY9 | ESOMEPRAZOLE MAGNESIUM | 217087-09-7 | Esomeprazole Magnesium |