Cephalexin
- Product NDC
- 70518-3595
- 11-digit product format
- 705183595
- Labeler code
- 70518
- Product ID
- 70518-3595_f0468186-c3fb-2030-e053-2995a90af3f2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cephalexin
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA062702
- Marketing category
- ANDA
- Marketing start
- 2022-12-13
- Marketing end
- 0000-00-00
- Substance
- CEPHALEXIN
- Active strength
- 250 mg/1
- Pharmacologic classes
- Cephalosporin Antibacterial [EPC], Cephalosporins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
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 | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-3595-0 | 70518359500 | 30 CAPSULE in 1 BLISTER PACK (70518-3595-0) | 30 capsule | 2022-12-13 | 0000-00-00 | No | No | Current |