Ceftriaxone
- Product NDC
- 63323-348
- 11-digit product format
- 633230348
- Labeler code
- 63323
- Product ID
- 63323-348_7e06a355-f45b-4e3c-e053-2a91aa0aeb9d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ceftriaxone
- Dosage form
- INJECTION, POWDER, FOR SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Fresenius Kabi USA, LLC
- Application
- ANDA065328
- Marketing category
- ANDA
- Marketing start
- 2011-06-20
- Marketing end
- 0000-00-00
- Substance
- CEFTRIAXONE 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