CEFAZOLIN
- Product NDC
- 52584-923
- 11-digit product format
- 525840923
- Labeler code
- 52584
- Product ID
- 52584-923_7b9d68f9-622d-4422-92a4-c100fc49ebbe
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- cefazolin
- Dosage form
- INJECTION, POWDER, FOR SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- General Injectables & Vaccines, Inc.
- Application
- ANDA065047
- Marketing category
- ANDA
- Marketing start
- 2019-12-30
- Marketing end
- 2024-11-30
- Substance
- CEFAZOLIN SODIUM
- Active strength
- 225 mg/mL
- Pharmacologic classes
- Cephalosporin Antibacterial [EPC], Cephalosporins [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 |
|---|
| 52584-923-90 | 52584092390 | 1 VIAL in 1 BAG (52584-923-90) > 2.2 mL in 1 VIAL | 1 vial | 2019-12-30 | 2024-11-30 | No | No | Current |