Esomeprazole Magnesium
- Product NDC
- 70518-3044
- 11-digit product format
- 705183044
- Labeler code
- 70518
- Product ID
- 70518-3044_beed13db-c911-138b-e053-2995a90a5c96
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Esomeprazole Magnesium
- Dosage form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA078279
- Marketing category
- ANDA
- Marketing start
- 2021-03-10
- Marketing end
- 0000-00-00
- Substance
- ESOMEPRAZOLE MAGNESIUM
- Active strength
- 40 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 |
|---|
| 70518-3044-0 | 70518304400 | 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-3044-0) | 2021-03-10 | 0000-00-00 | No | No | Current |
| 70518-3044-1 | 70518304401 | 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-3044-1) | 2021-04-01 | 0000-00-00 | No | No | Current |