Clindamycin Hydrochloride
- Product NDC
- 71335-1274
- 11-digit product format
- 713351274
- Labeler code
- 71335
- Product ID
- 71335-1274_7cf11341-78c5-44e2-903d-0f302e81e91c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clindamycin Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA063083
- Marketing category
- ANDA
- Marketing start
- 2014-09-09
- Marketing end
- 0000-00-00
- Substance
- CLINDAMYCIN HYDROCHLORIDE
- Active strength
- 300 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