Package 70518-4353-0

Brand: clindamycin hydrochloride

Generic: clindamycin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-4353-0
Digits Only 7051843530
Product NDC 70518-4353
Description

30 CAPSULE in 1 BLISTER PACK (70518-4353-0)

Marketing

Marketing Status
Marketed Since 2025-06-05
Brand clindamycin hydrochloride
Generic clindamycin hydrochloride
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "36d817ce-4ed6-8645-e063-6294a90ae853", "openfda": {"unii": ["T20OQ1YN1W"], "rxcui": ["197518"], "spl_set_id": ["fa084aad-07fa-44d2-8d01-d32f40acd2f3"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BLISTER PACK (70518-4353-0)", "package_ndc": "70518-4353-0", "marketing_start_date": "20250605"}], "brand_name": "Clindamycin Hydrochloride", "product_id": "70518-4353_36d817ce-4ed6-8645-e063-6294a90ae853", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Sebaceous Gland Activity [PE]", "Lincosamide Antibacterial [EPC]", "Lincosamides [CS]", "Neuromuscular Blockade [PE]"], "product_ndc": "70518-4353", "generic_name": "Clindamycin Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Clindamycin Hydrochloride", "active_ingredients": [{"name": "CLINDAMYCIN HYDROCHLORIDE", "strength": "150 mg/1"}], "application_number": "ANDA216957", "marketing_category": "ANDA", "marketing_start_date": "20250605", "listing_expiration_date": "20261231"}