Cefixime
- Product NDC
- 16714-766
- 11-digit product format
- 167140766
- Labeler code
- 16714
- Product ID
- 16714-766_f15f86c9-5ebe-800a-e053-2995a90af842
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- cefixime
- Dosage form
- POWDER, FOR SUSPENSION
- Route
- ORAL
- Labeler
- NorthStar RxLLC
- Application
- ANDA206938
- Marketing category
- ANDA
- Marketing start
- 2018-05-11
- Marketing end
- 0000-00-00
- Substance
- CEFIXIME
- Active strength
- 100 mg/5mL
- Pharmacologic classes
- Cephalosporin Antibacterial [EPC], Cephalosporins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2024-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 16714-766-01 | 16714076601 | 50 mL in 1 BOTTLE (16714-766-01) | 50 ml | 2018-05-11 | 0000-00-00 | No | No | Current |