cefdinir
- Product NDC
- 68788-8062
- 11-digit product format
- 687888062
- Labeler code
- 68788
- Product ID
- 68788-8062_7e9ca176-6bb8-49ea-a705-8a77cefd70d6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- cefdinir
- Dosage form
- POWDER, FOR SUSPENSION
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA210534
- Marketing category
- ANDA
- Marketing start
- 2021-08-13
- Marketing end
- 0000-00-00
- Substance
- CEFDINIR
- Active strength
- 250 mg/5mL
- 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 |
|---|
| 68788-8062 | CEFDINIR POWDER, FOR SUSPENSION [PREFERRED PHARMACEUTICALS INC.] | 5 | Legacy NDC | 20250221_43131b6b-6cda-4bb6-b73b-9cfeb314d4e2.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68788-8062-1 | 68788806201 | 100 mL in 1 BOTTLE (68788-8062-1) | 100 ml | 2021-08-13 | 0000-00-00 | No | No | Current |