Cefazolin
- Product NDC
- 84549-142
- 11-digit product format
- 845490142
- Labeler code
- 84549
- Product ID
- 84549-142_3d5cc73c-8a42-b285-e063-6294a90a609f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cefazolin
- Dosage form
- INJECTION, POWDER, FOR SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- ProPharma Distribution
- Application
- ANDA203661
- Marketing category
- ANDA
- Marketing start
- 2017-06-30
- Substance
- CEFAZOLIN SODIUM
- Active strength
- 1 g/1
- Pharmacologic classes
- Cephalosporin Antibacterial [EPC], Cephalosporins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Cefazolin
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| CEFAZOLIN SODIUM | 1 g/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | P380M0454Z |
| Rxcui | 1665050 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 84549-142-05 | Cefazolin | 1 in 1 VIAL, SINGLE-DOSE | INJECTION, POWDER, FOR SOLUTION | 1 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 84549-142-05 | 84549014205 | 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-DOSE (84549-142-05) | 2025-09-01 | No | No | Current |