CEFAZOLIN
- Product NDC
- 52584-087
- 11-digit product format
- 525840087
- Labeler code
- 52584
- Product ID
- 52584-087_3104e1a1-525e-4f0b-b406-39c633f5b795
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- cefazolin
- Dosage form
- INJECTION, POWDER, FOR SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- General Injectables & Vaccines, Inc.
- Application
- ANDA203661
- Marketing category
- ANDA
- Marketing start
- 2019-05-06
- Marketing end
- 2024-03-31
- Substance
- CEFAZOLIN 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 |
|---|
| 52584-087-00 | 52584008700 | 1 VIAL, SINGLE-DOSE in 1 BAG (52584-087-00) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-DOSE | 2019-05-06 | 2024-03-31 | No | No | Current |