Package 76282-744-05
Brand: tamsulosin hydrochloride
Generic: tamsulosin hydrochloridePackage Facts
Identity
Package NDC
76282-744-05
Digits Only
7628274405
Product NDC
76282-744
Description
500 CAPSULE in 1 BOTTLE (76282-744-05)
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": "06b18b22-60b7-486b-a87c-17a2ae4cfe41", "openfda": {"unii": ["11SV1951MR"], "rxcui": ["863669"], "spl_set_id": ["db6cb771-2cff-40b7-a5ef-ea3cf2a3b461"], "manufacturer_name": ["EXELAN PHARMACEUTICALS, INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 CAPSULE in 1 BOTTLE (76282-744-05)", "package_ndc": "76282-744-05", "marketing_start_date": "20240301"}, {"sample": false, "description": "90 CAPSULE in 1 BOTTLE (76282-744-90)", "package_ndc": "76282-744-90", "marketing_start_date": "20250314"}], "brand_name": "Tamsulosin hydrochloride", "product_id": "76282-744_06b18b22-60b7-486b-a87c-17a2ae4cfe41", "dosage_form": "CAPSULE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "76282-744", "generic_name": "Tamsulosin hydrochloride", "labeler_name": "EXELAN 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": "20240301", "listing_expiration_date": "20261231"}