Package 60760-598-90

Brand: tamsulosin hydrochloride

Generic: tamsulosin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 60760-598-90
Digits Only 6076059890
Product NDC 60760-598
Product ID 60760-598_8afa2b0c-1051-5021-e053-2995a90a056f
Description

90 CAPSULE in 1 BOTTLE, PLASTIC (60760-598-90)

Marketing

Marketing Status
Marketed Since 2017-12-26
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": "8afa2b0c-1051-5021-e053-2995a90a056f", "openfda": {"unii": ["11SV1951MR"], "rxcui": ["863669"], "spl_set_id": ["6142d7b6-e5ea-1af0-e053-2991aa0a00cd"], "manufacturer_name": ["St. Marys Medical Park Pharmacy"]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE in 1 BOTTLE, PLASTIC (60760-598-90)", "package_ndc": "60760-598-90", "marketing_start_date": "20171226"}], "brand_name": "Tamsulosin Hydrochloride", "product_id": "60760-598_8afa2b0c-1051-5021-e053-2995a90a056f", "dosage_form": "CAPSULE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "60760-598", "generic_name": "Tamsulosin Hydrochloride", "labeler_name": "St. Marys Medical Park Pharmacy", "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": "20171226", "listing_expiration_date": "20261231"}