Package 60760-450-90

Brand: tamsulosin hydrochloride

Generic: tamsulosin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 60760-450-90
Digits Only 6076045090
Product NDC 60760-450
Description

90 CAPSULE in 1 BOTTLE, PLASTIC (60760-450-90)

Marketing

Marketing Status
Marketed Since 2021-01-22
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": "b96a08ae-b256-caca-e053-2995a90ab659", "openfda": {"unii": ["11SV1951MR"], "rxcui": ["863669"], "spl_set_id": ["b969e0f3-1552-89d8-e053-2995a90acd7d"], "manufacturer_name": ["St. Mary's Medical Park Pharmacy"]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE in 1 BOTTLE, PLASTIC (60760-450-90)", "package_ndc": "60760-450-90", "marketing_start_date": "20210122"}], "brand_name": "Tamsulosin Hydrochloride", "product_id": "60760-450_b96a08ae-b256-caca-e053-2995a90ab659", "dosage_form": "CAPSULE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "60760-450", "generic_name": "Tamsulosin Hydrochloride", "labeler_name": "St. Mary's Medical Park Pharmacy", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tamsulosin Hydrochloride", "active_ingredients": [{"name": "TAMSULOSIN HYDROCHLORIDE", "strength": ".4 mg/1"}], "application_number": "ANDA204645", "marketing_category": "ANDA", "marketing_start_date": "20210122", "listing_expiration_date": "20261231"}