Clindamycin hydrochloride
- Product NDC
- 63629-8043
- 11-digit product format
- 636298043
- Labeler code
- 63629
- Product ID
- 63629-8043_87ed0660-9618-4f42-9d23-dcbe85b5e0ff
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clindamycin hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA065061
- Marketing category
- ANDA
- Marketing start
- 2001-03-23
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
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 | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-8043-1 | 63629804301 | 21 CAPSULE in 1 BOTTLE (63629-8043-1) | 21 capsule | 2019-07-18 | 0000-00-00 | No | No | Current |