Package 51655-957-26
Brand: verapamil hydrochloride
Generic: verapamil hydrochloridePackage Facts
Identity
Package NDC
51655-957-26
Digits Only
5165595726
Product NDC
51655-957
Description
90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-957-26)
Marketing
Marketing Status
Brand
verapamil hydrochloride
Generic
verapamil hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "49749ad1-b3e5-3e64-e063-6294a90a2eee", "openfda": {"unii": ["V3888OEY5R"], "rxcui": ["897666"], "spl_set_id": ["adc77fea-db39-aac5-e053-2995a90ad458"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-957-26)", "package_ndc": "51655-957-26", "marketing_start_date": "20200601"}], "brand_name": "Verapamil Hydrochloride", "product_id": "51655-957_49749ad1-b3e5-3e64-e063-6294a90a2eee", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Calcium Channel Blocker [EPC]", "Cytochrome P450 3A Inhibitors [MoA]", "Cytochrome P450 3A4 Inhibitors [MoA]", "P-Glycoprotein Inhibitors [MoA]"], "product_ndc": "51655-957", "generic_name": "Verapamil Hydrochloride", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Verapamil Hydrochloride", "active_ingredients": [{"name": "VERAPAMIL HYDROCHLORIDE", "strength": "120 mg/1"}], "application_number": "ANDA070994", "marketing_category": "ANDA", "marketing_start_date": "20200601", "listing_expiration_date": "20271231"}