Esomeprazole sodium
- Product NDC
- 16729-252
- 11-digit product format
- 167290252
- Labeler code
- 16729
- Product ID
- 16729-252_aedd1bd2-0e7f-3e54-e053-2a95a90aa65e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Esomeprazole sodium
- Dosage form
- INJECTION
- Route
- INTRAVENOUS
- Labeler
- Accord Healthcare Inc.
- Application
- ANDA205379
- Marketing category
- ANDA
- Marketing start
- 2016-10-11
- Marketing end
- 0000-00-00
- Substance
- ESOMEPRAZOLE SODIUM
- Active strength
- 40 mg/5mL
- Pharmacologic classes
- Proton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA],Cytochrome P450 2C19 Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 16729-252-66 | 16729025266 | 1 VIAL in 1 CARTON (16729-252-66) > 5 mL in 1 VIAL | 1 vial | 2016-10-11 | 0000-00-00 | No | No | Current |
| 16729-252-69 | 16729025269 | 10 VIAL in 1 CARTON (16729-252-69) > 5 mL in 1 VIAL | 10 vial | 2016-10-11 | 0000-00-00 | No | No | Current |