Cefazolin Sodium
- Product NDC
- 72189-584
- 11-digit product format
- 721890584
- Labeler code
- 72189
- Product ID
- 72189-584_22dfc2e4-07a8-8d13-e063-6394a90a3e9f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cefazolin Sodium
- Dosage form
- INJECTION, POWDER, FOR SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Direct_rx
- Application
- ANDA203661
- Marketing category
- ANDA
- Marketing start
- 2024-09-24
- 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 Sodium
- 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 |
|---|
| 72189-584-01 | Cefazolin Sodium | 1 in 1 CARTON | INJECTION, POWDER, FOR SOLUTION | 1 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72189-584 | CEFAZOLIN SODIUM INJECTION, POWDER, FOR SOLUTION [DIRECT_RX] | 1 | Current NDC, 1 package rows | 20240926_22dfc2e4-07a7-8d13-e063-6394a90a3e9f.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 72189-584-01 | 72189058401 | 1 INJECTION, POWDER, FOR SOLUTION in 1 CARTON (72189-584-01) | 2024-09-24 | No | No | Current |