Cefazolin
- Product NDC
- 50090-4256
- 11-digit product format
- 500904256
- Labeler code
- 50090
- Product ID
- 50090-4256_9f453c63-7855-47c4-9ac8-adb3cbe1bb26
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cefazolin
- Dosage form
- INJECTION, POWDER, FOR SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- A-S Medication Solutions
- Application
- ANDA065047
- Marketing category
- ANDA
- Marketing start
- 2001-09-18
- Substance
- CEFAZOLIN SODIUM
- Active strength
- 330 mg/mL
- Pharmacologic classes
- Cephalosporin Antibacterial [EPC], Cephalosporins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| P380M0454Z | CEFAZOLIN SODIUM | 27164-46-1 | CEFAZOLIN SODIUM |
| IHS69L0Y4T | CEFAZOLIN | 25953-19-9 | Cefazolin |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 50090-4256-0 | 50090425600 | 25 VIAL in 1 BOX (50090-4256-0) / 3 mL in 1 VIAL | 25 vial | 2019-04-05 | No | No | Historical |