CEFTRIAXONE
- Product NDC
- 63187-435
- 11-digit product format
- 631870435
- Labeler code
- 63187
- Product ID
- 63187-435_a9795cfb-d225-46e6-b081-68a14e996c27
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- CEFTRIAXONE
- Dosage form
- INJECTION, POWDER, FOR SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Proficient Rx LP
- Application
- ANDA065125
- Marketing category
- ANDA
- Marketing start
- 2009-06-01
- Marketing end
- 2022-12-31
- Substance
- CEFTRIAXONE SODIUM
- Active strength
- 1 g/1
- Pharmacologic classes
- Cephalosporin Antibacterial [EPC], Cephalosporins [CS]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63187-435-01 | 63187043501 | 1 INJECTION, POWDER, FOR SOLUTION in 1 BOX (63187-435-01) | 2015-02-02 | 0000-00-00 | No | No | Current |