Package 70518-0074-1

Brand: terazosin

Generic: terazosin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-0074-1
Digits Only 7051800741
Product NDC 70518-0074
Description

30 CAPSULE in 1 BLISTER PACK (70518-0074-1)

Marketing

Marketing Status
Marketed Since 2021-03-24
Brand terazosin
Generic terazosin hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "47e23176-6018-48b8-e063-6394a90afff8", "openfda": {"unii": ["D32S14F082"], "rxcui": ["313217"], "spl_set_id": ["a3a5901a-6395-4030-a27b-1fb17cd97315"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BLISTER PACK (70518-0074-1)", "package_ndc": "70518-0074-1", "marketing_start_date": "20210324"}], "brand_name": "Terazosin", "product_id": "70518-0074_47e23176-6018-48b8-e063-6394a90afff8", "dosage_form": "CAPSULE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "70518-0074", "generic_name": "Terazosin Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Terazosin", "active_ingredients": [{"name": "TERAZOSIN HYDROCHLORIDE", "strength": "2 mg/1"}], "application_number": "ANDA075317", "marketing_category": "ANDA", "marketing_start_date": "20161221", "listing_expiration_date": "20271231"}