Cephalexin
- Product NDC
- 71335-2976
- 11-digit product format
- 713352976
- Labeler code
- 71335
- Product ID
- 71335-2976_4bb520de-2294-4f6e-b5a6-e8c64683f856
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cephalexin
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA065253
- Marketing category
- ANDA
- Marketing start
- 2005-11-16
- Substance
- CEPHALEXIN
- Active strength
- 500 mg/1
- Pharmacologic classes
- Cephalosporin Antibacterial [EPC], Cephalosporins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| OBN7UDS42Y | CEPHALEXIN | 23325-78-2 | CEPHALEXIN |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71335-2976-1 | 71335297601 | 12 CAPSULE in 1 BOTTLE (71335-2976-1) | 12 capsule | 2025-11-06 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Cephalexin | Bryant Ranch Prepack | 2025-11-06 | HUMAN PRESCRIPTION DRUG LABEL | 1 |