Clindamycin Phosphate and Benzoyl Peroxide
- Product NDC
- 0781-7161
- 11-digit product format
- 007817161
- Labeler code
- 0781
- Product ID
- 0781-7161_b5c8681b-5513-4d3e-90dc-9d11d8c1799c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clindamycin Phosphate and Benzoyl Peroxide
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Sandoz Inc.
- Application
- ANDA203688
- Marketing category
- ANDA
- Marketing start
- 2016-08-25
- Marketing end
- 0000-00-00
- Substance
- CLINDAMYCIN PHOSPHATE; BENZOYL PEROXIDE
- Active strength
- 12 mg/g; mg/g
- Pharmacologic classes
- Decreased Sebaceous Gland Activity [PE],Lincosamide Antibacterial [EPC],Lincosamides [CS]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 0781-7161-19 | 00781716119 | 1 TUBE in 1 CARTON (0781-7161-19) > 45 g in 1 TUBE | 1 tube | 2016-08-25 | 0000-00-00 | No | No | Current |