cephalexin
- Product NDC
- 68071-3587
- 11-digit product format
- 680713587
- Labeler code
- 68071
- Product ID
- 68071-3587_141bc1c6-156c-65ca-e063-6394a90a5d9b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cephalexin
- Dosage form
- FOR SUSPENSION
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA065234
- Marketing category
- ANDA
- Marketing start
- 2017-09-06
- Substance
- CEPHALEXIN
- Active strength
- 250 mg/5mL
- 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 |
|---|
| 68071-3587-2 | 68071358702 | 200 mL in 1 BOTTLE (68071-3587-2) | 200 ml | 2024-03-20 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| cephalexin | NuCare Pharmaceuticals,Inc. | 2024-03-20 | HUMAN PRESCRIPTION DRUG LABEL | 1 |