AMPICILLIN
- Product NDC
- 52584-114
- 11-digit product format
- 525840114
- Labeler code
- 52584
- Product ID
- 52584-114_df06aa40-d908-4f2d-9460-af4c8d54863b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- AMPICILLIN SODIUM
- Dosage form
- INJECTION, POWDER, FOR SOLUTION
- Route
- INTRAVENOUS
- Labeler
- General Injectables and Vaccines, Inc.
- Application
- ANDA065499
- Marketing category
- ANDA
- Marketing start
- 2018-07-02
- Marketing end
- 2023-11-30
- Substance
- AMPICILLIN SODIUM
- Active strength
- 2 g/1
- Pharmacologic classes
- Penicillin-class Antibacterial [EPC], Penicillins [CS]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 52584-114-20 | 52584011420 | 1 VIAL in 1 BAG (52584-114-20) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL | 1 vial | 2018-07-02 | 0000-00-00 | No | No | Current |