Package 71335-1967-1

Brand: potassium citrate

Generic: potassium citrate
NDC Package

Package Facts

Identity

Package NDC 71335-1967-1
Digits Only 7133519671
Product NDC 71335-1967
Product ID 71335-1967_09e72ff9-f66c-46be-aae4-ba650a4215a8
Description

30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1967-1)

Marketing

Marketing Status
Marketed Since 2021-10-04
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": "09e72ff9-f66c-46be-aae4-ba650a4215a8", "openfda": {"unii": ["EE90ONI6FF"], "rxcui": ["199381"], "spl_set_id": ["ff67f638-5b53-406a-962a-87773a91fc48"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1967-1)", "package_ndc": "71335-1967-1", "marketing_start_date": "20211004"}], "brand_name": "Potassium Citrate", "product_id": "71335-1967_09e72ff9-f66c-46be-aae4-ba650a4215a8", "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": "71335-1967", "generic_name": "Potassium Citrate", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Citrate", "active_ingredients": [{"name": "POTASSIUM CITRATE", "strength": "10 meq/1"}], "application_number": "ANDA212779", "marketing_category": "ANDA", "marketing_start_date": "20200316", "listing_expiration_date": "20261231"}