cefazolin
- Product NDC
- 25021-100
- 11-digit product format
- 250210100
- Labeler code
- 25021
- Product ID
- 25021-100_6dfa594e-90e8-4085-af30-6d3660a6bebf
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- cefazolin sodium
- Dosage form
- INJECTION, POWDER, FOR SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Sagent Pharmaceuticals
- Application
- ANDA065303
- Marketing category
- ANDA
- Marketing start
- 2009-02-01
- Marketing end
- 0000-00-00
- Substance
- CEFAZOLIN SODIUM
- Active strength
- 500 mg/2.2mL
- Pharmacologic classes
- Cephalosporin Antibacterial [EPC],Cephalosporins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 25021-100 | CEFAZOLIN (CEFAZOLIN SODIUM) INJECTION, POWDER, FOR SOLUTION [SAGENT PHARMACEUTICALS] | 14 | Legacy NDC | 20240302_e8f40f72-3cf0-43dc-a797-fb98dd8af228.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 25021-100-10 | 25021010010 | 25 VIAL in 1 CARTON (25021-100-10) > 2.2 mL in 1 VIAL | 25 vial | 2009-02-01 | 0000-00-00 | No | No | Current |
| 25021-100-66 | 25021010066 | 25 VIAL in 1 CARTON (25021-100-66) > 2.2 mL in 1 VIAL | 25 vial | 2015-07-01 | 0000-00-00 | No | No | Current |