Clindamycin Hydrochloride
- Product NDC
- 42292-018
- 11-digit product format
- 422920018
- Labeler code
- 42292
- Product ID
- 42292-018_9aee45ba-92b5-0837-e053-2a95a90ad834
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clindamycin Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Mylan Institutional Inc.
- Application
- ANDA065442
- Marketing category
- ANDA
- Marketing start
- 2016-09-22
- Marketing end
- 2021-01-31
- 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
- 0000-00-00
- Current FDA listing
- Historical FDA.report record