Cefazolin
- Product NDC
- 55154-7826
- 11-digit product format
- 551547826
- Labeler code
- 55154
- Product ID
- 55154-7826_f0f192cd-52c6-45b5-ab01-fb1cc83cb59d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cefazolin
- Dosage form
- INJECTION, POWDER, FOR SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Cardinal Health
- Application
- ANDA065226
- Marketing category
- ANDA
- Marketing start
- 2009-03-27
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record