Package 68382-132-14
Brand: tamsulosin hydrochloride
Generic: tamsulosin hydrochloridePackage Facts
Identity
Package NDC
68382-132-14
Digits Only
6838213214
Product NDC
68382-132
Description
60 CAPSULE in 1 BOTTLE (68382-132-14)
Marketing
Marketing Status
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": "ee9d9efd-0c79-4993-bfd7-d4c30e20bddd", "openfda": {"unii": ["11SV1951MR"], "rxcui": ["863669"], "spl_set_id": ["300be29a-c56d-4daa-ba89-f207c281ea20"], "manufacturer_name": ["Zydus Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (68382-132-01)", "package_ndc": "68382-132-01", "marketing_start_date": "20100427"}, {"sample": false, "description": "500 CAPSULE in 1 BOTTLE (68382-132-05)", "package_ndc": "68382-132-05", "marketing_start_date": "20100427"}, {"sample": false, "description": "30 CAPSULE in 1 BOTTLE (68382-132-06)", "package_ndc": "68382-132-06", "marketing_start_date": "20100427"}, {"sample": false, "description": "1000 CAPSULE in 1 BOTTLE (68382-132-10)", "package_ndc": "68382-132-10", "marketing_start_date": "20100427"}, {"sample": false, "description": "60 CAPSULE in 1 BOTTLE (68382-132-14)", "package_ndc": "68382-132-14", "marketing_start_date": "20100427"}, {"sample": false, "description": "90 CAPSULE in 1 BOTTLE (68382-132-16)", "package_ndc": "68382-132-16", "marketing_start_date": "20100427"}, {"sample": false, "description": "100 BLISTER PACK in 1 CARTON (68382-132-77) / 1 CAPSULE in 1 BLISTER PACK (68382-132-30)", "package_ndc": "68382-132-77", "marketing_start_date": "20100427"}], "brand_name": "Tamsulosin Hydrochloride", "product_id": "68382-132_ee9d9efd-0c79-4993-bfd7-d4c30e20bddd", "dosage_form": "CAPSULE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "68382-132", "generic_name": "Tamsulosin Hydrochloride", "labeler_name": "Zydus Pharmaceuticals USA Inc.", "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": "20100427", "listing_expiration_date": "20261231"}