Cephalexin
- Product NDC
- 72162-2145
- 11-digit product format
- 721622145
- Labeler code
- 72162
- Product ID
- 72162-2145_58759ee9-29d7-4b3e-8b95-d4857eeffadd
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cephalexin
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA062702
- Marketing category
- ANDA
- Marketing start
- 1990-09-30
- 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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Cephalexin
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| CEPHALEXIN | 500 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | OBN7UDS42Y |
| Rxcui | 309114 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72162-2145-5 | 72162214505 | 500 CAPSULE in 1 BOTTLE (72162-2145-5) | 500 capsule | 2023-12-07 | No | No | Historical |