Cefazolin
- Product NDC
- 52584-100
- 11-digit product format
- 525840100
- Labeler code
- 52584
- Product ID
- 52584-100_276f669a-f3b2-4e67-a91a-26e4ce7f131b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cefazolin
- Dosage form
- INJECTION, POWDER, FOR SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- General Injectables and Vaccines, Inc.
- Application
- ANDA065303
- Marketing category
- ANDA
- Marketing start
- 2017-02-15
- Marketing end
- 2022-03-31
- Substance
- CEFAZOLIN SODIUM
- Active strength
- 500 mg/2.2mL
- 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 |
|---|
| 52584-100-10 | 52584010010 | 1 VIAL in 1 BAG (52584-100-10) > 2.2 mL in 1 VIAL | 1 vial | 2017-02-15 | 2022-03-31 | No | No | Current |