Clindamycin hydrochloride
- Product NDC
- 68071-3939
- 11-digit product format
- 680713939
- Labeler code
- 68071
- Product ID
- 68071-3939_4730b7b9-dfc8-6605-e063-6294a90a006c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clindamycin hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals, Inc.
- Application
- ANDA065061
- Marketing category
- ANDA
- Marketing start
- 2001-03-23
- Substance
- CLINDAMYCIN HYDROCHLORIDE
- Active strength
- 150 mg/1
- 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 |
|---|
| T20OQ1YN1W | CLINDAMYCIN HYDROCHLORIDE | 21462-39-5 | CLINDAMYCIN HYDROCHLORIDE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 68071-3939-6 | 68071393906 | 6 CAPSULE in 1 BOTTLE (68071-3939-6) | 6 capsule | 2025-12-30 | No | No | Historical |