Package 42291-989-10

Brand: tamsulosin hydrochloride

Generic: tamsulosin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 42291-989-10
Digits Only 4229198910
Product NDC 42291-989
Description

1000 CAPSULE in 1 BOTTLE (42291-989-10)

Marketing

Marketing Status
Marketed Since 2025-11-16
Brand tamsulosin hydrochloride
Generic tamsulosin hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "43bec92e-7ee1-85d6-e063-6394a90a3167", "openfda": {"unii": ["11SV1951MR"], "rxcui": ["863669"], "spl_set_id": ["43bec742-fbc4-39af-e063-6294a90ac734"], "manufacturer_name": ["AvKARE"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 CAPSULE in 1 BOTTLE (42291-989-10)", "package_ndc": "42291-989-10", "marketing_start_date": "20251116"}, {"sample": false, "description": "90 CAPSULE in 1 BOTTLE (42291-989-90)", "package_ndc": "42291-989-90", "marketing_start_date": "20251116"}], "brand_name": "Tamsulosin Hydrochloride", "product_id": "42291-989_43bec92e-7ee1-85d6-e063-6394a90a3167", "dosage_form": "CAPSULE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "42291-989", "generic_name": "TAMSULOSIN HYDROCHLORIDE", "labeler_name": "AvKARE", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tamsulosin Hydrochloride", "active_ingredients": [{"name": "TAMSULOSIN HYDROCHLORIDE", "strength": ".4 mg/1"}], "application_number": "ANDA090377", "marketing_category": "ANDA", "marketing_start_date": "20251116", "listing_expiration_date": "20261231"}