Cephalexin
- Product NDC
- 48102-021
- 11-digit product format
- 481020021
- Labeler code
- 48102
- Product ID
- 48102-021_14e38252-0bad-4c3e-a489-f45eb4631feb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- CEPHALEXIN
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Fera Pharmaceuticals, LLC
- Application
- NDA050405
- Marketing category
- NDA
- Marketing start
- 2017-06-02
- Marketing end
- 2021-12-31
- Substance
- CEPHALEXIN
- Active strength
- 750 mg/1
- Pharmacologic classes
- Cephalosporin Antibacterial [EPC],Cephalosporins [CS]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 48102-021-20 | 48102002120 | 20 CAPSULE in 1 BOTTLE (48102-021-20) | 20 capsule | 2019-09-10 | 2021-12-31 | No | No | Current |
| 48102-021-50 | 48102002150 | 50 CAPSULE in 1 BOTTLE (48102-021-50) | 50 capsule | 2017-06-02 | 2021-12-31 | No | No | Current |