Cefdinir
- Product NDC
- 70518-2537
- 11-digit product format
- 705182537
- Labeler code
- 70518
- Product ID
- 70518-2537_dc23fdc1-d32b-1da5-e053-2a95a90a7767
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cefdinir
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA065434
- Marketing category
- ANDA
- Marketing start
- 2020-01-11
- Marketing end
- 0000-00-00
- Substance
- CEFDINIR
- Active strength
- 300 mg/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 |
|---|
| 70518-2537 | CEFDINIR CAPSULE [REMEDYREPACK INC.] | 10 | Legacy NDC | 20250112_dff50439-0005-485e-b36e-33cd068b4939.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-2537-0 | 70518253700 | 20 CAPSULE in 1 BOTTLE, PLASTIC (70518-2537-0) | 20 capsule | 2020-01-11 | 0000-00-00 | No | No | Current |