Clindamycin Hydrochloride
- Product NDC
- 70518-0238
- 11-digit product format
- 705180238
- Labeler code
- 70518
- Product ID
- 70518-0238_8350b902-7f12-c5a0-e053-2a91aa0a930d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clindamycin Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA063029
- Marketing category
- ANDA
- Marketing start
- 2017-02-20
- 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