Clindamycin Hydrochloride
- Product NDC
- 0713-3171
- 11-digit product format
- 007133171
- Labeler code
- 0713
- Product ID
- 0713-3171_76f81cef-1b34-4263-aec8-d17feef008ac
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clindamycin Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Cosette Pharmaceuticals, Inc.
- Application
- ANDA063029
- Marketing category
- ANDA
- Marketing start
- 2016-03-14
- Marketing end
- 0000-00-00
- Substance
- CLINDAMYCIN HYDROCHLORIDE
- Active strength
- 150 mg/1
- Pharmacologic classes
- Decreased Sebaceous Gland Activity [PE],Lincosamide Antibacterial [EPC],Lincosamides [CS]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0713-3171-01 | 00713317101 | 100 CAPSULE in 1 BOTTLE (0713-3171-01) | 100 capsule | 2016-03-14 | 0000-00-00 | No | No | Current |