Ceftriaxone
- Product NDC
- 60505-0753
- 11-digit product format
- 605050753
- Labeler code
- 60505
- Product ID
- 60505-0753_faa4586e-499f-4a88-8047-41e5f042eb62
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ceftriaxone
- Dosage form
- INJECTION, POWDER, FOR SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Apotex Corporation
- Application
- ANDA065230
- Marketing category
- ANDA
- Marketing start
- 2005-08-02
- Marketing end
- 0000-00-00
- Substance
- CEFTRIAXONE SODIUM
- Active strength
- 2 g/1
- Pharmacologic classes
- Cephalosporin Antibacterial [EPC],Cephalosporins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record