Package 0527-2801-32

Brand: vardenafil hydrochloride

Generic: vardenafil hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0527-2801-32
Digits Only 0527280132
Product NDC 0527-2801
Description

30 TABLET in 1 BOTTLE (0527-2801-32)

Marketing

Marketing Status
Marketed Since 2018-11-01
Brand vardenafil hydrochloride
Generic vardenafil hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0a6ac33c-4a1f-4d07-b60e-453bb7111c9f", "openfda": {"upc": ["0305272802322"], "unii": ["5M8S2CU0TS"], "rxcui": ["349478", "349479", "349480", "402273"], "spl_set_id": ["2782efed-6198-47b9-81ac-3e255e2ab7f6"], "manufacturer_name": ["Lannett Company, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (0527-2801-32)", "package_ndc": "0527-2801-32", "marketing_start_date": "20181101"}], "brand_name": "Vardenafil Hydrochloride", "product_id": "0527-2801_0a6ac33c-4a1f-4d07-b60e-453bb7111c9f", "dosage_form": "TABLET", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "0527-2801", "generic_name": "Vardenafil Hydrochloride", "labeler_name": "Lannett Company, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Vardenafil Hydrochloride", "active_ingredients": [{"name": "VARDENAFIL HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA209057", "marketing_category": "ANDA", "marketing_start_date": "20181101", "listing_expiration_date": "20261231"}