Clindamycin Phosphate and Benzoyl Peroxide
- Product NDC
- 72162-2077
- 11-digit product format
- 721622077
- Labeler code
- 72162
- Product ID
- 72162-2077_1ce2692a-4384-4f6c-9de3-491692751388
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clindamycin Phosphate, Benzoyl Peroxide
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA205397
- Marketing category
- ANDA
- Marketing start
- 2019-09-12
- Substance
- BENZOYL PEROXIDE; CLINDAMYCIN PHOSPHATE
- Active strength
- 25; 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 | Marketing start | Sample | Exclude flag | Status |
|---|
| 72162-2077-1 | 72162207701 | 1 BOTTLE, PUMP in 1 CARTON (72162-2077-1) / 50 g in 1 BOTTLE, PUMP | 2023-08-16 | No | No | Historical |