Package 0904-7383-61

Brand: tamsulosin hydrochloride

Generic: tamsulosin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0904-7383-61
Digits Only 0904738361
Product NDC 0904-7383
Product ID 0904-7383_dbf1ae34-50e3-4c54-8e4f-fef014455f3b
Description

100 BLISTER PACK in 1 CARTON (0904-7383-61) / 1 CAPSULE in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2023-10-02
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": "dbf1ae34-50e3-4c54-8e4f-fef014455f3b", "openfda": {"unii": ["11SV1951MR"], "rxcui": ["863669"], "spl_set_id": ["f8302a6e-b8da-4931-a279-b49e37943816"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (0904-7383-61)  / 1 CAPSULE in 1 BLISTER PACK", "package_ndc": "0904-7383-61", "marketing_start_date": "20231002"}], "brand_name": "Tamsulosin Hydrochloride", "product_id": "0904-7383_dbf1ae34-50e3-4c54-8e4f-fef014455f3b", "dosage_form": "CAPSULE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "0904-7383", "generic_name": "Tamsulosin Hydrochloride", "labeler_name": "Major Pharmaceuticals", "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"}