Package 63672-0021-9

Brand: tamsulosin hydrochloride

Generic: tamsulosin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63672-0021-9
Digits Only 6367200219
Product NDC 63672-0021
Product ID 63672-0021_44e3098a-c374-d7aa-e063-6294a90aef5d
Description

20000 CAPSULE in 1 DRUM (63672-0021-9)

Marketing

Marketing Status
Marketed Since 2024-01-15
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": "44e3098a-c374-d7aa-e063-6294a90aef5d", "openfda": {"unii": ["11SV1951MR"], "rxcui": ["863669"], "spl_set_id": ["13a5032d-0be1-4001-916e-459f0b1a051d"], "manufacturer_name": ["Synthon Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "20000 CAPSULE in 1 DRUM (63672-0021-9)", "package_ndc": "63672-0021-9", "marketing_start_date": "20240115"}], "brand_name": "Tamsulosin hydrochloride", "product_id": "63672-0021_44e3098a-c374-d7aa-e063-6294a90aef5d", "dosage_form": "CAPSULE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "63672-0021", "generic_name": "tamsulosin hydrochloride", "labeler_name": "Synthon Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tamsulosin hydrochloride", "active_ingredients": [{"name": "TAMSULOSIN HYDROCHLORIDE", "strength": ".4 mg/1"}], "application_number": "ANDA078801", "marketing_category": "ANDA", "marketing_start_date": "20100427", "listing_expiration_date": "20261231"}