Package 67296-2131-2

Brand: potassium chloride

Generic: potassium chloride
NDC Package

Package Facts

Identity

Package NDC 67296-2131-2
Digits Only 6729621312
Product NDC 67296-2131
Product ID 67296-2131_46ac9fcf-f297-e94a-e063-6294a90ab7ec
Description

20 TABLET, EXTENDED RELEASE in 1 BOTTLE (67296-2131-2)

Marketing

Marketing Status
Marketed Since 2016-07-26
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": "46ac9fcf-f297-e94a-e063-6294a90ab7ec", "openfda": {"upc": ["0368462471012", "0368462472019"], "unii": ["660YQ98I10"], "rxcui": ["1801294"], "spl_set_id": ["3735d41a-7787-6b92-e063-6294a90add45"], "manufacturer_name": ["Redpharm Drug"]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, EXTENDED RELEASE in 1 BOTTLE (67296-2131-2)", "package_ndc": "67296-2131-2", "marketing_start_date": "20160726"}], "brand_name": "potassium chloride", "product_id": "67296-2131_46ac9fcf-f297-e94a-e063-6294a90ab7ec", "dosage_form": "TABLET, 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": "67296-2131", "generic_name": "potassium chloride", "labeler_name": "Redpharm Drug", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "potassium chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "1500 mg/1"}], "application_number": "ANDA203562", "marketing_category": "ANDA", "marketing_start_date": "20160726", "listing_expiration_date": "20261231"}