Clindamycin Phosphate and Benzoyl Peroxide
- Product NDC
- 63629-8798
- 11-digit product format
- 636298798
- Labeler code
- 63629
- Product ID
- 63629-8798_3086e241-9de2-490a-8f3a-ba7bea79e6fe
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clindamycin Phosphate and Benzoyl Peroxide
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA203688
- Marketing category
- ANDA
- Marketing start
- 2016-08-25
- Marketing end
- 0000-00-00
- Substance
- BENZOYL PEROXIDE; CLINDAMYCIN PHOSPHATE
- Active strength
- 50 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-8798-1 | 63629879801 | 1 TUBE in 1 CARTON (63629-8798-1) > 45 g in 1 TUBE | 1 tube | 2021-09-10 | 0000-00-00 | No | No | Current |