Package 51655-832-52

Brand: tamsulosin hydrochloride

Generic: tamsulosin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 51655-832-52
Digits Only 5165583252
Product NDC 51655-832
Description

30 CAPSULE in 1 BOTTLE, PLASTIC (51655-832-52)

Marketing

Marketing Status
Marketed Since 2022-02-23
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": "4973d0cd-3f6d-fb42-e063-6294a90a0882", "openfda": {"unii": ["11SV1951MR"], "rxcui": ["863669"], "spl_set_id": ["d9df4fe0-90ab-0d96-e053-2a95a90a5ff1"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE in 1 BOTTLE, PLASTIC (51655-832-26)", "package_ndc": "51655-832-26", "marketing_start_date": "20220923"}, {"sample": false, "description": "30 CAPSULE in 1 BOTTLE, PLASTIC (51655-832-52)", "package_ndc": "51655-832-52", "marketing_start_date": "20220223"}], "brand_name": "Tamsulosin Hydrochloride", "product_id": "51655-832_4973d0cd-3f6d-fb42-e063-6294a90a0882", "dosage_form": "CAPSULE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "51655-832", "generic_name": "Tamsulosin Hydrochloride", "labeler_name": "Northwind Health Company, LLC", "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": "20220223", "listing_expiration_date": "20271231"}