Cefazolin
- Product NDC
- 70518-3047
- 11-digit product format
- 705183047
- Labeler code
- 70518
- Product ID
- 70518-3047_e531fa0b-244a-f490-e053-2a95a90af0b3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cefazolin
- Dosage form
- INJECTION, POWDER, FOR SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA203661
- Marketing category
- ANDA
- Marketing start
- 2021-03-12
- Marketing end
- 0000-00-00
- Substance
- CEFAZOLIN SODIUM
- Active strength
- 1 g/1
- Pharmacologic classes
- Cephalosporin Antibacterial [EPC], Cephalosporins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70518-3047 | CEFAZOLIN INJECTION, POWDER, FOR SOLUTION [REMEDYREPACK INC.] | 6 | Legacy NDC | 20250418_ec3063e4-b639-4606-9f2e-daa2bb28567e.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-3047-0 | 70518304700 | 25 VIAL, SINGLE-DOSE in 1 CARTON (70518-3047-0) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-DOSE (70518-3047-1) | 2021-03-12 | 0000-00-00 | No | No | Current |