Clindamycin Hydrochloride
- Product NDC
- 70518-0598
- 11-digit product format
- 705180598
- Labeler code
- 70518
- Product ID
- 70518-0598_86410121-d4c0-8ebf-e053-2a91aa0ab05f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clindamycin Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA065243
- Marketing category
- ANDA
- Marketing start
- 2017-06-28
- 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