Cefazolin
- Product NDC
- 60505-6094
- 11-digit product format
- 605056094
- Labeler code
- 60505
- Product ID
- 60505-6094_75247770-da12-442e-a1a6-f293f52ede97
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cefazolin
- Dosage form
- INJECTION, POWDER, FOR SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Apotex Corporation
- Application
- ANDA065247
- Marketing category
- ANDA
- Marketing start
- 2012-04-20
- Marketing end
- 0000-00-00
- Substance
- CEFAZOLIN SODIUM
- Active strength
- 10 g/1
- Pharmacologic classes
- Cephalosporin Antibacterial [EPC],Cephalosporins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record