Package 31722-130-01

Brand: potassium citrate

Generic: potassium citrate
NDC Package

Package Facts

Identity

Package NDC 31722-130-01
Digits Only 3172213001
Product NDC 31722-130
Product ID 31722-130_cb7e4f56-0ffe-4809-991c-1751b62e63c7
Description

100 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-130-01)

Marketing

Marketing Status
Marketed Since 2021-02-15
Brand potassium citrate
Generic potassium citrate
Sample Package No

Linked Drug Pages (1)

POTASSIUM CITRATE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "cb7e4f56-0ffe-4809-991c-1751b62e63c7", "openfda": {"upc": ["0331722130011", "0331722129015", "0331722132015"], "unii": ["EE90ONI6FF"], "rxcui": ["199376", "199381", "898490"], "spl_set_id": ["ea933654-e8d2-4662-9a9a-4a6d79a9fb20"], "manufacturer_name": ["Camber Pharmaceuticals, Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-130-01)", "package_ndc": "31722-130-01", "marketing_start_date": "20210215"}], "brand_name": "POTASSIUM CITRATE", "product_id": "31722-130_cb7e4f56-0ffe-4809-991c-1751b62e63c7", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Acidifying Activity [MoA]", "Anti-coagulant [EPC]", "Calcium Chelating Activity [MoA]", "Calculi Dissolution Agent [EPC]", "Decreased Coagulation Factor Activity [PE]"], "product_ndc": "31722-130", "generic_name": "Potassium Citrate", "labeler_name": "Camber Pharmaceuticals, Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "POTASSIUM CITRATE", "active_ingredients": [{"name": "POTASSIUM CITRATE", "strength": "10 meq/1"}], "application_number": "ANDA214420", "marketing_category": "ANDA", "marketing_start_date": "20210215", "listing_expiration_date": "20261231"}