Package 71335-2897-1

Brand: potassium citrate

Generic: potassium citrate
NDC Package

Package Facts

Identity

Package NDC 71335-2897-1
Digits Only 7133528971
Product NDC 71335-2897
Description

100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2897-1)

Marketing

Marketing Status
Marketed Since 2025-10-23
Brand potassium citrate
Generic potassium citrate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "41d908e6-82e7-3ae6-e063-6294a90aeb03", "openfda": {"unii": ["EE90ONI6FF"], "rxcui": ["898490"], "spl_set_id": ["b3ccba22-48cd-45f8-8c72-b80f34fe56be"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2897-1)", "package_ndc": "71335-2897-1", "marketing_start_date": "20251023"}], "brand_name": "POTASSIUM CITRATE", "product_id": "71335-2897_41d908e6-82e7-3ae6-e063-6294a90aeb03", "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": "71335-2897", "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": "15 meq/1"}], "application_number": "ANDA214420", "marketing_category": "ANDA", "marketing_start_date": "20210215", "listing_expiration_date": "20261231"}