Cephalexin
- Product NDC
- 68788-8986
- 11-digit product format
- 687888986
- Labeler code
- 68788
- Product ID
- 68788-8986_003dd9a0-3e9a-45bf-8a04-974206094b4c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cephalexin
- Dosage form
- POWDER, FOR SUSPENSION
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA065326
- Marketing category
- ANDA
- Marketing start
- 2016-02-01
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 68788-8986-1 | 68788898601 | 100 mL in 1 BOTTLE (68788-8986-1) | 100 ml | 2016-02-01 | 0000-00-00 | No | No | Current |
| 68788-8986-2 | 68788898602 | 200 mL in 1 BOTTLE (68788-8986-2) | 200 ml | 2016-02-01 | 0000-00-00 | No | No | Current |