Clindamycin Hydrochloride
- Product NDC
- 42291-389
- 11-digit product format
- 422910389
- Labeler code
- 42291
- Product ID
- 42291-389_73a79494-27e4-4706-e053-2a91aa0a5f7c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clindamycin Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- AvKARE, Inc.
- Application
- ANDA063083
- Marketing category
- ANDA
- Marketing start
- 2018-08-21
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record