Package 33342-203-37
Brand: vardenafil
Generic: vardenafilPackage Facts
Identity
Package NDC
33342-203-37
Digits Only
3334220337
Product NDC
33342-203
Description
1 BLISTER PACK in 1 CARTON (33342-203-37) / 4 TABLET in 1 BLISTER PACK
Marketing
Marketing Status
Brand
vardenafil
Generic
vardenafil
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "695d5a7e-546f-4e86-8edc-3c32e1d3bb19", "openfda": {"unii": ["5M8S2CU0TS"], "rxcui": ["996179"], "spl_set_id": ["0ad213e0-d18a-4e67-a405-df95322eaa52"], "manufacturer_name": ["Macleods Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (33342-203-37) / 4 TABLET in 1 BLISTER PACK", "package_ndc": "33342-203-37", "marketing_start_date": "20181026"}], "brand_name": "Vardenafil", "product_id": "33342-203_695d5a7e-546f-4e86-8edc-3c32e1d3bb19", "dosage_form": "TABLET", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "33342-203", "generic_name": "Vardenafil", "labeler_name": "Macleods Pharmaceuticals Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Vardenafil", "active_ingredients": [{"name": "VARDENAFIL HYDROCHLORIDE TRIHYDRATE", "strength": "11.85 mg/1"}], "application_number": "ANDA205988", "marketing_category": "ANDA", "marketing_start_date": "20181026", "listing_expiration_date": "20261231"}