Cefepime
- Product NDC
- 71288-020
- 11-digit product format
- 712880020
- Labeler code
- 71288
- Product ID
- 71288-020_29116a89-8b37-4fd0-b0b8-5f42d3e63228
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- cefepime hydrochloride
- Dosage form
- INJECTION, POWDER, FOR SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Meitheal Pharmaceuticals Inc.
- Application
- ANDA212721
- Marketing category
- ANDA
- Marketing start
- 2020-07-21
- Marketing end
- 0000-00-00
- Substance
- CEFEPIME HYDROCHLORIDE
- Active strength
- 1 g/1
- Pharmacologic classes
- Cephalosporin Antibacterial [EPC],Cephalosporins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 71288-020-16 | 71288002016 | 10 VIAL, SINGLE-DOSE in 1 CARTON (71288-020-16) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-DOSE (71288-020-15) | 2020-07-21 | 0000-00-00 | No | No | Current |