Cephalexin
- Product NDC
- 68071-4233
- 11-digit product format
- 680714233
- Labeler code
- 68071
- Product ID
- 68071-4233_bb77740d-0edf-a5d4-e053-2a95a90a3ad6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cephalexin
- Dosage form
- POWDER, FOR SUSPENSION
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA065326
- Marketing category
- ANDA
- Marketing start
- 2007-04-12
- Marketing end
- 0000-00-00
- Substance
- CEPHALEXIN
- Active strength
- 250 mg/5mL
- Pharmacologic classes
- Cephalosporin Antibacterial [EPC],Cephalosporins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-4233-0 | 68071423300 | 100 mL in 1 BOTTLE (68071-4233-0) | 100 ml | 2018-01-15 | 0000-00-00 | No | No | Current |