Package 0781-2076-10

Brand: tamsulosin hydrochloride

Generic: tamsulosin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0781-2076-10
Digits Only 0781207610
Product NDC 0781-2076
Product ID 0781-2076_98c2abd9-1998-48cd-83f9-f5f94ff39345
Description

1000 CAPSULE in 1 BOTTLE (0781-2076-10)

Marketing

Marketing Status
Marketed Since 2010-04-27
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": "98c2abd9-1998-48cd-83f9-f5f94ff39345", "openfda": {"unii": ["11SV1951MR"], "rxcui": ["863669"], "spl_set_id": ["fb120098-b007-4a33-80b8-b7279c7668ee"], "manufacturer_name": ["Sandoz Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (0781-2076-01)", "package_ndc": "0781-2076-01", "marketing_start_date": "20100427"}, {"sample": false, "description": "1000 CAPSULE in 1 BOTTLE (0781-2076-10)", "package_ndc": "0781-2076-10", "marketing_start_date": "20100427"}, {"sample": false, "description": "90 CAPSULE in 1 BOTTLE (0781-2076-92)", "package_ndc": "0781-2076-92", "marketing_start_date": "20190131"}], "brand_name": "tamsulosin hydrochloride", "product_id": "0781-2076_98c2abd9-1998-48cd-83f9-f5f94ff39345", "dosage_form": "CAPSULE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "0781-2076", "generic_name": "tamsulosin hydrochloride", "labeler_name": "Sandoz Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "tamsulosin hydrochloride", "active_ingredients": [{"name": "TAMSULOSIN HYDROCHLORIDE", "strength": ".4 mg/1"}], "application_number": "ANDA078015", "marketing_category": "ANDA", "marketing_start_date": "20100427", "listing_expiration_date": "20261231"}