potassium citrate

Generic: potassium citrate

Labeler: remedyrepack inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name potassium citrate
Generic Name potassium citrate
Labeler remedyrepack inc.
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

potassium citrate 10 meq/1

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-4477
Product ID 70518-4477_3e9891d0-97b9-ccd1-e063-6394a90ae2cd
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA214420
Listing Expiration 2026-12-31
Marketing Start 2025-09-12

Pharmacologic Class

Classes
acidifying activity [moa] anti-coagulant [epc] calcium chelating activity [moa] calculi dissolution agent [epc] decreased coagulation factor activity [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 705184477
Hyphenated Format 70518-4477

Supplemental Identifiers

RxCUI
199381
UNII
EE90ONI6FF

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name potassium citrate (source: ndc)
Generic Name potassium citrate (source: ndc)
Application Number ANDA214420 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 meq/1
source: ndc
Packaging
  • 100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-4477-0)
source: ndc

Packages (1)

70518-4477-0 100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-4477-0)

Ingredients (1)

potassium citrate (10 meq/1)

Linked Drug Pages (1)

POTASSIUM CITRATE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3e9891d0-97b9-ccd1-e063-6394a90ae2cd", "openfda": {"unii": ["EE90ONI6FF"], "rxcui": ["199381"], "spl_set_id": ["08c769d4-1dc0-4130-8f9c-cddace13a79b"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-4477-0)", "package_ndc": "70518-4477-0", "marketing_start_date": "20250912"}], "brand_name": "POTASSIUM CITRATE", "product_id": "70518-4477_3e9891d0-97b9-ccd1-e063-6394a90ae2cd", "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": "70518-4477", "generic_name": "Potassium Citrate", "labeler_name": "REMEDYREPACK 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": "20250912", "listing_expiration_date": "20261231"}