Package 51655-915-52

Brand: terazosin

Generic: terazosin
NDC Package

Package Facts

Identity

Package NDC 51655-915-52
Digits Only 5165591552
Product NDC 51655-915
Product ID 51655-915_49741c96-db68-402a-e063-6394a90a07e4
Description

30 CAPSULE in 1 BOTTLE, PLASTIC (51655-915-52)

Marketing

Marketing Status
Marketed Since 2023-06-26
Brand terazosin
Generic terazosin
Sample Package No

Linked Drug Pages (1)

terazosin ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "49741c96-db68-402a-e063-6394a90a07e4", "openfda": {"unii": ["D32S14F082"], "rxcui": ["313217"], "spl_set_id": ["ff0efbc2-d7aa-9783-e053-6394a90a384f"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE, PLASTIC (51655-915-52)", "package_ndc": "51655-915-52", "marketing_start_date": "20230626"}], "brand_name": "terazosin", "product_id": "51655-915_49741c96-db68-402a-e063-6394a90a07e4", "dosage_form": "CAPSULE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "51655-915", "generic_name": "terazosin", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "terazosin", "active_ingredients": [{"name": "TERAZOSIN HYDROCHLORIDE", "strength": "2 mg/1"}], "application_number": "ANDA075614", "marketing_category": "ANDA", "marketing_start_date": "20230626", "listing_expiration_date": "20271231"}