AMPICILLIN
- Product NDC
- 52584-350
- 11-digit product format
- 525840350
- Labeler code
- 52584
- Product ID
- 52584-350_c78ce237-8097-46e7-a833-793b8c2b00ed
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- AMPICILLIN
- Dosage form
- INJECTION, POWDER, FOR SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- General Injectables and Vaccines, Inc.
- Application
- ANDA201025
- Marketing category
- ANDA
- Marketing start
- 2019-07-15
- Marketing end
- 0000-00-00
- Substance
- AMPICILLIN SODIUM
- Active strength
- 500 mg/1
- Pharmacologic classes
- Penicillin-class Antibacterial [EPC],Penicillins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 52584-350-50 | 52584035050 | 1 VIAL in 1 BAG (52584-350-50) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL | 1 vial | 2019-07-15 | 0000-00-00 | No | No | Current |