Cephalexin
- Product NDC
- 72162-1833
- 11-digit product format
- 721621833
- Labeler code
- 72162
- Product ID
- 72162-1833_44f4e82f-3f80-4a1a-af11-7b5c909d662d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cephalexin
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA090836
- Marketing category
- ANDA
- Marketing start
- 2012-06-04
- Substance
- CEPHALEXIN
- Active strength
- 750 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 |
|---|
| 72162-1833-2 | 72162183302 | 50 CAPSULE in 1 BOTTLE (72162-1833-2) | 50 capsule | 2023-04-18 | No | No | Historical |
| 72162-1833-4 | 72162183304 | 20 CAPSULE in 1 BOTTLE (72162-1833-4) | 20 capsule | 2023-04-18 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Cephalexin | Bryant Ranch Prepack | 2024-08-08 | HUMAN PRESCRIPTION DRUG LABEL | 102 |