Cephalexin
- Product NDC
- 70518-4511
- 11-digit product format
- 705184511
- Labeler code
- 70518
- Product ID
- 70518-4511_42397ed1-11b3-2036-e063-6294a90adb46
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cephalexin
- Dosage form
- FOR SUSPENSION
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA210221
- Marketing category
- ANDA
- Marketing start
- 2025-10-28
- 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 |
|---|
| 70518-4511-0 | 70518451100 | 100 mL in 1 BOTTLE (70518-4511-0) | 100 ml | 2025-10-28 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Cephalexin | REMEDYREPACK INC. | 2025-10-28 | HUMAN PRESCRIPTION DRUG LABEL | 1 |