Cefazolin
- Product NDC
- 52584-023
- 11-digit product format
- 525840023
- Labeler code
- 52584
- Product ID
- 52584-023_4554932c-ada2-4c18-8651-3795bf75278a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cefazolin Sodium
- Dosage form
- INJECTION, POWDER, FOR SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- General Injectables & Vaccines, Inc
- Application
- ANDA065226
- Marketing category
- ANDA
- Marketing start
- 2011-09-07
- Marketing end
- 0000-00-00
- Substance
- CEFAZOLIN SODIUM
- Active strength
- 1 g/3mL
- Pharmacologic classes
- Cephalosporin Antibacterial [EPC],Cephalosporins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record