Esomeprazole Magnesium
- Product NDC
- 70677-0069
- 11-digit product format
- 706770069
- Labeler code
- 70677
- Product ID
- 70677-0069_bd82c2b6-f0d7-4209-afeb-dbc38ee47250
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Esomeprazole Magnesium
- Dosage form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Labeler
- McKESSON Corporation
- Application
- ANDA209339
- Marketing category
- ANDA
- Marketing start
- 2017-10-16
- Marketing end
- 0000-00-00
- Substance
- ESOMEPRAZOLE MAGNESIUM DIHYDRATE
- Active strength
- 20 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record