esomeprazole magnesium
- Product NDC
- 69844-031
- 11-digit product format
- 698440031
- Labeler code
- 69844
- Product ID
- 69844-031_34f2102a-fed6-4057-8a93-29377a66693c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- esomeprazole magnesium
- Dosage form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Graviti Pharmaceuticals Private Limited
- Application
- ANDA213486
- Marketing category
- ANDA
- Marketing start
- 2021-03-19
- Marketing end
- 0000-00-00
- Substance
- ESOMEPRAZOLE MAGNESIUM
- Active strength
- 20 mg/1
- Pharmacologic classes
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 69844-031-01 | 69844003101 | 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (69844-031-01) | 2021-03-19 | 0000-00-00 | No | No | Current |
| 69844-031-02 | 69844003102 | 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (69844-031-02) | 2021-03-19 | 0000-00-00 | No | No | Current |
| 69844-031-03 | 69844003103 | 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (69844-031-03) | 2021-03-19 | 0000-00-00 | No | No | Current |