Package 46708-235-04

Brand: vardenafil

Generic: vardenafil
NDC Package

Package Facts

Identity

Package NDC 46708-235-04
Digits Only 4670823504
Product NDC 46708-235
Product ID 46708-235_2ca8929b-0b62-4302-9ab4-60ad3768e803
Description

4 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (46708-235-04)

Marketing

Marketing Status
Marketed Since 2018-11-20
Brand vardenafil
Generic vardenafil
Sample Package No

Linked Drug Pages (1)

Vardenafil ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2ca8929b-0b62-4302-9ab4-60ad3768e803", "openfda": {"unii": ["5M8S2CU0TS"], "rxcui": ["996179"], "spl_set_id": ["dce0b31b-4522-4cb4-9dba-3aea2b2bb082"], "manufacturer_name": ["Alembic Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "4 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (46708-235-04)", "package_ndc": "46708-235-04", "marketing_start_date": "20181120"}], "brand_name": "Vardenafil", "product_id": "46708-235_2ca8929b-0b62-4302-9ab4-60ad3768e803", "dosage_form": "TABLET, ORALLY DISINTEGRATING", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "46708-235", "generic_name": "Vardenafil", "labeler_name": "Alembic Pharmaceuticals Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Vardenafil", "active_ingredients": [{"name": "VARDENAFIL HYDROCHLORIDE TRIHYDRATE", "strength": "10 mg/1"}], "application_number": "ANDA208324", "marketing_category": "ANDA", "marketing_start_date": "20181120", "listing_expiration_date": "20261231"}