Clindamycin hydrochloride
- Product NDC
- 55700-328
- 11-digit product format
- 557000328
- Labeler code
- 55700
- Product ID
- 55700-328_8a9182f9-25a7-4478-91c3-78181407ade8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clindamycin hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- 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
- 2019-12-31
- 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 |