Package 62135-864-30
Brand: vardenafil hydrochloride
Generic: vardenafil hydrochloridePackage Facts
Identity
Package NDC
62135-864-30
Digits Only
6213586430
Product NDC
62135-864
Description
30 TABLET in 1 BOTTLE (62135-864-30)
Marketing
Marketing Status
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": "459d49f5-7be3-8f85-e063-6294a90a2064", "openfda": {"upc": ["0362135864309"], "unii": ["5M8S2CU0TS"], "rxcui": ["402273"], "spl_set_id": ["57a0c163-a5e8-4c6e-a4ea-114cb2668407"], "manufacturer_name": ["Chartwell RX, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (62135-864-30)", "package_ndc": "62135-864-30", "marketing_start_date": "20240226"}], "brand_name": "Vardenafil Hydrochloride", "product_id": "62135-864_459d49f5-7be3-8f85-e063-6294a90a2064", "dosage_form": "TABLET", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "62135-864", "generic_name": "Vardenafil Hydrochloride", "labeler_name": "Chartwell RX, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Vardenafil Hydrochloride", "active_ingredients": [{"name": "VARDENAFIL HYDROCHLORIDE", "strength": "2.5 mg/1"}], "application_number": "ANDA209057", "marketing_category": "ANDA", "marketing_start_date": "20181031", "listing_expiration_date": "20261231"}