Cefazolin
- Product NDC
- 60505-6142
- 11-digit product format
- 605056142
- Labeler code
- 60505
- Product ID
- 60505-6142_10b501ca-c77f-4b3f-85df-ddf2715bfcd0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cefazolin
- Dosage form
- INJECTION, POWDER, FOR SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Apotex Corp.
- 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, 1665060, 2630753 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 60505-6142-0 | Cefazolin | 1 in 1 VIAL, SINGLE-DOSE | INJECTION, POWDER, FOR SOLUTION | 1 | | 13 |
| 60505-6142-5 | Cefazolin | 25 in 1 CARTON | INJECTION, POWDER, FOR SOLUTION | 25 | | 13 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 60505-6142 | CEFAZOLIN INJECTION, POWDER, FOR SOLUTION [APOTEX CORP.] | 12 | Current NDC, Legacy NDC, 2 package rows | 20240220_0422fe47-c372-494f-bac2-612f550b44a4.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 |
|---|
| 60505-6142-0 | 60505614200 | 1 in 1 VIAL, SINGLE-DOSE | | | | | Historical |
| 60505-6142-5 | 60505614205 | 25 VIAL, SINGLE-DOSE in 1 CARTON (60505-6142-5) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-DOSE (60505-6142-0) | 2017-06-30 | 0000-00-00 | No | No | Current |