Package 62135-579-12

Brand: hydralazine hydrochloride

Generic: hydralazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 62135-579-12
Digits Only 6213557912
Product NDC 62135-579
Product ID 62135-579_459c0193-3a85-878d-e063-6294a90afc31
Description

120 TABLET, FILM COATED in 1 BOTTLE (62135-579-12)

Marketing

Marketing Status
Marketed Since 2023-05-09
Brand hydralazine hydrochloride
Generic hydralazine hydrochloride
Sample Package No

Linked Drug Pages (1)

Hydralazine Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "459c0193-3a85-878d-e063-6294a90afc31", "openfda": {"upc": ["0362135580124", "0362135581121", "0362135582128", "0362135579128"], "unii": ["FD171B778Y"], "rxcui": ["905199", "905222", "905225", "905395"], "spl_set_id": ["0c7f9bd0-6c0a-4521-b77a-3582faa96874"], "manufacturer_name": ["Chartwell RX, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "120 TABLET, FILM COATED in 1 BOTTLE (62135-579-12)", "package_ndc": "62135-579-12", "marketing_start_date": "20230509"}], "brand_name": "Hydralazine Hydrochloride", "product_id": "62135-579_459c0193-3a85-878d-e063-6294a90afc31", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Arteriolar Vasodilation [PE]", "Arteriolar Vasodilator [EPC]"], "product_ndc": "62135-579", "generic_name": "Hydralazine Hydrochloride", "labeler_name": "Chartwell RX, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydralazine Hydrochloride", "active_ingredients": [{"name": "HYDRALAZINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA086242", "marketing_category": "ANDA", "marketing_start_date": "20070406", "listing_expiration_date": "20261231"}