Package 0904-7216-61

Brand: potassium chloride

Generic: potassium chloride
NDC Package

Package Facts

Identity

Package NDC 0904-7216-61
Digits Only 0904721661
Product NDC 0904-7216
Product ID 0904-7216_9d5dc98f-9e9a-4303-8f20-446e84da3fcf
Description

100 BLISTER PACK in 1 CARTON (0904-7216-61) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2018-12-19
Brand potassium chloride
Generic potassium chloride
Sample Package No

Linked Drug Pages (1)

Potassium Chloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "9d5dc98f-9e9a-4303-8f20-446e84da3fcf", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["628953"], "spl_set_id": ["a9d68a40-75e3-4c5c-b5d7-1d6160527fa7"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (0904-7216-61)  / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "0904-7216-61", "marketing_start_date": "20181219"}], "brand_name": "Potassium Chloride", "product_id": "0904-7216_9d5dc98f-9e9a-4303-8f20-446e84da3fcf", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Increased Large Intestinal Motility [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]", "Potassium Compounds [CS]", "Potassium Salt [EPC]"], "product_ndc": "0904-7216", "generic_name": "Potassium Chloride", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "750 mg/1"}], "application_number": "ANDA210921", "marketing_category": "ANDA", "marketing_start_date": "20181219", "listing_expiration_date": "20261231"}