Package 62756-160-83

Brand: tamsulosin hydrochloride

Generic: tamsulosin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 62756-160-83
Digits Only 6275616083
Product NDC 62756-160
Product ID 62756-160_52595417-3e2e-4d58-9167-dd5b2bf1b082
Description

30 CAPSULE in 1 BOTTLE (62756-160-83)

Marketing

Marketing Status
Marketed Since 2010-07-15
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": "52595417-3e2e-4d58-9167-dd5b2bf1b082", "openfda": {"upc": ["0362756160811"], "unii": ["11SV1951MR"], "rxcui": ["863669"], "spl_set_id": ["d742707b-4c17-4b08-a9d0-491ba2bf6415"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (62756-160-08)", "package_ndc": "62756-160-08", "marketing_start_date": "20100715"}, {"sample": false, "description": "500 CAPSULE in 1 BOTTLE (62756-160-13)", "package_ndc": "62756-160-13", "marketing_start_date": "20100715"}, {"sample": false, "description": "1000 CAPSULE in 1 BOTTLE (62756-160-18)", "package_ndc": "62756-160-18", "marketing_start_date": "20100715"}, {"sample": false, "description": "90 CAPSULE in 1 BOTTLE (62756-160-81)", "package_ndc": "62756-160-81", "marketing_start_date": "20100715"}, {"sample": false, "description": "30 CAPSULE in 1 BOTTLE (62756-160-83)", "package_ndc": "62756-160-83", "marketing_start_date": "20100715"}, {"sample": false, "description": "100 CAPSULE in 1 BOTTLE (62756-160-88)", "package_ndc": "62756-160-88", "marketing_start_date": "20100715"}], "brand_name": "Tamsulosin Hydrochloride", "product_id": "62756-160_52595417-3e2e-4d58-9167-dd5b2bf1b082", "dosage_form": "CAPSULE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "62756-160", "generic_name": "Tamsulosin Hydrochloride", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tamsulosin Hydrochloride", "active_ingredients": [{"name": "TAMSULOSIN HYDROCHLORIDE", "strength": ".4 mg/1"}], "application_number": "ANDA090931", "marketing_category": "ANDA", "marketing_start_date": "20100715", "listing_expiration_date": "20261231"}