potassium citrate extended release (42543-408)

Drug Facts

Product Profile

Brand Name potassium citrate extended release

Generic Name potassium citrate

Labeler strides pharma inc.

Dosage Form TABLET

Routes

ORAL

Active Ingredients

potassium citrate 15 meq/1

Manufacturer

Strides Pharma Inc.

Identifiers & Regulatory

Product NDC 42543-408

Product ID 42543-408_67ba2683-6fb5-429e-ab39-6f004ac33f1b

Product Type HUMAN PRESCRIPTION DRUG

Marketing Category ANDA

Application Number ANDA206813

Listing Expiration 2026-12-31

Marketing Start 2017-11-01

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 42543408

Hyphenated Format 42543-408

Supplemental Identifiers

RxCUI

199376 199381 898490

UNII

EE90ONI6FF

Packaging Origin

Original Packager

true

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 extended release (source: ndc)

Generic Name potassium citrate (source: ndc)

Application Number ANDA206813 (source: ndc)

Routes

ORAL

source: ndc

Resolved Composition

Strengths

15 meq/1

source: ndc

Packaging

100 TABLET in 1 BOTTLE (42543-408-01)

source: ndc

Packages (1)

42543-408-01 100 TABLET in 1 BOTTLE (42543-408-01)

Ingredients (1)

potassium citrate (15 meq/1)

Linked Drug Pages (1)

POTASSIUM CITRATE EXTENDED RELEASE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload

{"route": ["ORAL"], "spl_id": "67ba2683-6fb5-429e-ab39-6f004ac33f1b", "openfda": {"unii": ["EE90ONI6FF"], "rxcui": ["199376", "199381", "898490"], "spl_set_id": ["5f38b02c-703c-4fc2-b833-654e41bd617f"], "manufacturer_name": ["Strides Pharma Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (42543-408-01)", "package_ndc": "42543-408-01", "marketing_start_date": "20171101"}], "brand_name": "POTASSIUM CITRATE EXTENDED RELEASE", "product_id": "42543-408_67ba2683-6fb5-429e-ab39-6f004ac33f1b", "dosage_form": "TABLET", "pharm_class": ["Acidifying Activity [MoA]", "Anti-coagulant [EPC]", "Calcium Chelating Activity [MoA]", "Calculi Dissolution Agent [EPC]", "Decreased Coagulation Factor Activity [PE]"], "product_ndc": "42543-408", "generic_name": "POTASSIUM CITRATE", "labeler_name": "Strides Pharma Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "POTASSIUM CITRATE", "brand_name_suffix": "EXTENDED RELEASE", "active_ingredients": [{"name": "POTASSIUM CITRATE", "strength": "15 meq/1"}], "application_number": "ANDA206813", "marketing_category": "ANDA", "marketing_start_date": "20171101", "listing_expiration_date": "20261231"}