Cefixime
- Product NDC
- 62250-668
- 11-digit product format
- 622500668
- Labeler code
- 62250
- Product ID
- 62250-668_efe464ad-36be-7101-e053-2995a90a5c1f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- cefixime
- Dosage form
- POWDER, FOR SUSPENSION
- Route
- ORAL
- Labeler
- Belcher Pharmaceuticals,LLC
- Application
- ANDA206939
- Marketing category
- ANDA
- Marketing start
- 2017-03-15
- Marketing end
- 0000-00-00
- Substance
- CEFIXIME
- Active strength
- 500 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
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 62250-668 | CEFIXIME POWDER, FOR SUSPENSION [BELCHER PHARMACEUTICALS,LLC] | 10 | Legacy NDC | 20250213_ef6f6181-baa6-4896-abfa-2097afe1f087.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 62250-668-24 | 62250066824 | 10 mL in 1 BOTTLE (62250-668-24) | 10 ml | 2017-03-15 | 0000-00-00 | No | No | Current |
| 62250-668-25 | 62250066825 | 20 mL in 1 BOTTLE (62250-668-25) | 20 ml | 2017-03-15 | 0000-00-00 | No | No | Current |