Package 82009-025-10

Brand: tamsulosin hydrochloride

Generic: tamsulosin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 82009-025-10
Digits Only 8200902510
Product NDC 82009-025
Product ID 82009-025_82b44507-051f-4892-a0b7-ed3955c2f72f
Description

1000 CAPSULE in 1 BOTTLE (82009-025-10)

Marketing

Marketing Status
Marketed Since 2022-08-20
Brand tamsulosin hydrochloride
Generic tamsulosin hydrochloride
Sample Package No

Linked Drug Pages (1)

Tamsulosin Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "82b44507-051f-4892-a0b7-ed3955c2f72f", "openfda": {"upc": ["0382009025100"], "unii": ["11SV1951MR"], "rxcui": ["863669"], "spl_set_id": ["12ba3063-a134-41e2-8447-45933d4f0f58"], "manufacturer_name": ["Quallent Pharmaceuticals Health LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 CAPSULE in 1 BOTTLE (82009-025-10)", "package_ndc": "82009-025-10", "marketing_start_date": "20220820"}], "brand_name": "Tamsulosin Hydrochloride", "product_id": "82009-025_82b44507-051f-4892-a0b7-ed3955c2f72f", "dosage_form": "CAPSULE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "82009-025", "generic_name": "Tamsulosin Hydrochloride", "labeler_name": "Quallent Pharmaceuticals Health LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tamsulosin Hydrochloride", "active_ingredients": [{"name": "TAMSULOSIN HYDROCHLORIDE", "strength": ".4 mg/1"}], "application_number": "ANDA078225", "marketing_category": "ANDA", "marketing_start_date": "20220820", "listing_expiration_date": "20261231"}