Cefixime
- Product NDC
- 62250-664
- 11-digit product format
- 622500664
- Labeler code
- 62250
- Product ID
- 62250-664_efe45e1a-35b7-0a0d-e053-2a95a90aff45
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- cefixime
- Dosage form
- POWDER, FOR SUSPENSION
- Route
- ORAL
- Labeler
- Belcher Pharmaceuticals,LLC
- Application
- ANDA206938
- Marketing category
- ANDA
- Marketing start
- 2017-03-15
- Marketing end
- 0000-00-00
- Substance
- CEFIXIME
- Active strength
- 200 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 |
|---|
| 62250-664 | CEFIXIME POWDER, FOR SUSPENSION [BELCHER PHARMACEUTICALS,LLC] | 11 | Legacy NDC | 20250213_54db9828-803c-4e82-8202-cee919330786.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 62250-664-26 | 62250066426 | 50 mL in 1 BOTTLE (62250-664-26) | 50 ml | 2017-03-15 | 0000-00-00 | No | No | Current |
| 62250-664-27 | 62250066427 | 75 mL in 1 BOTTLE (62250-664-27) | 75 ml | 2017-03-15 | 0000-00-00 | No | No | Current |
| 62250-664-28 | 62250066428 | 100 mL in 1 BOTTLE (62250-664-28) | 100 ml | 2017-03-15 | 0000-00-00 | No | No | Current |