Cefazolin
- Product NDC
- 0143-9140
- 11-digit product format
- 001439140
- Labeler code
- 0143
- Product ID
- 0143-9140_e32063de-96fe-4fb4-9176-5a9d6dc4a722
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cefazolin
- Dosage form
- INJECTION, POWDER, FOR SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Hikma Pharmaceuticals USA Inc.
- Application
- NDA216109
- Marketing category
- NDA
- Marketing start
- 2023-03-01
- Substance
- CEFAZOLIN SODIUM
- Active strength
- 3 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 | 3 g/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | P380M0454Z |
| Rxcui | 1665060, 2630753 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0143-9140-25 | Cefazolin | 25 in 1 CARTON | INJECTION, POWDER, FOR SOLUTION | 25 | | 13 |
| 0143-9140-25 | Cefazolin | 1 in 1 VIAL | INJECTION, POWDER, FOR SOLUTION | 1 | | 13 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0143-9140 | CEFAZOLIN INJECTION, POWDER, FOR SOLUTION [HIKMA PHARMACEUTICALS USA INC.] | 12 | Current NDC, 2 package rows | 20240417_6c7761d3-c154-4802-9876-627cd42913f0.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 0143-9140-25 | 00143914025 | 25 VIAL in 1 CARTON (0143-9140-25) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL | 25 vial | 2023-03-01 | No | No | Current |