Cefazolin
- Product NDC
- 0143-9665
- 11-digit product format
- 001439665
- Labeler code
- 0143
- Product ID
- 0143-9665_a1fc6bdd-6f1b-402f-9e84-b6e5ed5febb4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cefazolin
- Dosage form
- INJECTION, POWDER, FOR SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Hikma Pharmaceuticals USA Inc.
- Application
- ANDA065143
- Marketing category
- ANDA
- Marketing start
- 2004-10-18
- Substance
- CEFAZOLIN SODIUM
- Active strength
- 20 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 | 20 g/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | P380M0454Z |
| Rxcui | 313920 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0143-9665-10 | Cefazolin | 1 in 1 VIAL | INJECTION, POWDER, FOR SOLUTION | 1 | | 15 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0143-9665 | CEFAZOLIN INJECTION, POWDER, FOR SOLUTION [HIKMA PHARMACEUTICALS USA INC.] | 15 | Current NDC, Legacy NDC, 1 package rows | 20240420_06091653-e568-4e82-acc7-aefbce16de17.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0143-9665-10 | 00143966510 | 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (0143-9665-10) | 2004-10-18 | 0000-00-00 | No | No | Current |