cephalexin
- Product NDC
- 68788-7938
- 11-digit product format
- 687887938
- Labeler code
- 68788
- Product ID
- 68788-7938_cc261896-91d9-406b-ae36-70a409938101
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cephalexin
- Dosage form
- FOR SUSPENSION
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA065234
- Marketing category
- ANDA
- Marketing start
- 2021-06-16
- 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
- 2023-12-31
- 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 |
|---|
| 68788-7938-1 | 68788793801 | 100 mL in 1 BOTTLE (68788-7938-1) | 100 ml | 2021-06-16 | 0000-00-00 | No | No | Current |
| 68788-7938-2 | 68788793802 | 200 mL in 1 BOTTLE (68788-7938-2) | 200 ml | 2021-06-16 | 0000-00-00 | No | No | Current |