CLINDAMYCIN PHOSPHATE AND BENZOYL PEROXIDE
- Product NDC
- 71335-2878
- 11-digit product format
- 713352878
- Labeler code
- 71335
- Product ID
- 71335-2878_110c76ed-44cb-4dd5-9213-bd92cc756440
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- CLINDAMYCIN PHOSPHATE AND BENZOYL PEROXIDE
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA212433
- Marketing category
- ANDA
- Marketing start
- 2021-05-20
- Substance
- BENZOYL PEROXIDE; CLINDAMYCIN PHOSPHATE
- Active strength
- 50; 10 mg/g; mg/g
- Pharmacologic classes
- Decreased Sebaceous Gland Activity [PE], Lincosamide Antibacterial [EPC], Lincosamides [CS], Neuromuscular Blockade [PE]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| W9WZN9A0GM | BENZOYL PEROXIDE | 94-36-0 | BENZOYL PEROXIDE |
| EH6D7113I8 | CLINDAMYCIN PHOSPHATE | 24729-96-2 | CLINDAMYCIN PHOSPHATE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71335-2878-1 | 71335287801 | 1 TUBE in 1 CARTON (71335-2878-1) / 45 g in 1 TUBE | 1 tube | 2025-10-22 | No | No | Historical |