Package 63323-614-06

Brand: hydralazine hydrochloride

Generic: hydralazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63323-614-06
Digits Only 6332361406
Product NDC 63323-614
Description

25 VIAL, SINGLE-DOSE in 1 CARTON (63323-614-06) / 1 mL in 1 VIAL, SINGLE-DOSE (63323-614-03)

Marketing

Marketing Status
Marketed Since 2001-09-05
Brand hydralazine hydrochloride
Generic hydralazine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "bf1b7c2f-535c-45bb-928a-65606d87685e", "openfda": {"upc": ["0363323614034"], "unii": ["FD171B778Y"], "rxcui": ["966571"], "spl_set_id": ["bf1b7c2f-535c-45bb-928a-65606d87685e"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, SINGLE-DOSE in 1 CARTON (63323-614-06)  / 1 mL in 1 VIAL, SINGLE-DOSE (63323-614-03)", "package_ndc": "63323-614-06", "marketing_start_date": "20010905"}], "brand_name": "Hydralazine Hydrochloride", "product_id": "63323-614_bf1b7c2f-535c-45bb-928a-65606d87685e", "dosage_form": "INJECTION", "pharm_class": ["Arteriolar Vasodilation [PE]", "Arteriolar Vasodilator [EPC]"], "product_ndc": "63323-614", "generic_name": "HYDRALAZINE HYDROCHLORIDE", "labeler_name": "Fresenius Kabi USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydralazine Hydrochloride", "active_ingredients": [{"name": "HYDRALAZINE HYDROCHLORIDE", "strength": "20 mg/mL"}], "application_number": "ANDA040388", "marketing_category": "ANDA", "marketing_start_date": "20010905", "listing_expiration_date": "20261231"}