Package 50090-6700-0

Brand: tamsulosin hydrochloride

Generic: tamsulosin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50090-6700-0
Digits Only 5009067000
Product NDC 50090-6700
Product ID 50090-6700_72dc02ce-ddf8-451e-a4ae-569220e3cf6c
Description

90 CAPSULE in 1 BOTTLE (50090-6700-0)

Marketing

Marketing Status
Marketed Since 2023-09-22
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": "72dc02ce-ddf8-451e-a4ae-569220e3cf6c", "openfda": {"unii": ["11SV1951MR"], "rxcui": ["863669"], "spl_set_id": ["00bb2d71-1f21-494c-aa66-a82be3a0a8e6"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE in 1 BOTTLE (50090-6700-0)", "package_ndc": "50090-6700-0", "marketing_start_date": "20230922"}], "brand_name": "Tamsulosin Hydrochloride", "product_id": "50090-6700_72dc02ce-ddf8-451e-a4ae-569220e3cf6c", "dosage_form": "CAPSULE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "50090-6700", "generic_name": "Tamsulosin Hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tamsulosin Hydrochloride", "active_ingredients": [{"name": "TAMSULOSIN HYDROCHLORIDE", "strength": ".4 mg/1"}], "application_number": "ANDA202433", "marketing_category": "ANDA", "marketing_start_date": "20130430", "listing_expiration_date": "20261231"}