potassium citrate

Generic: potassium citrate

Labeler: rising pharma holdings, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

potassium citrate 540 mg/1

Manufacturer
Rising Pharma Holdings, Inc.

Identifiers & Regulatory

Product NDC 16571-864
Product ID 16571-864_2e4e8acc-d3ad-4246-bd65-d95691896fc8
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077440
Listing Expiration 2027-12-31
Marketing Start 2024-12-15

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 16571864
Hyphenated Format 16571-864

Supplemental Identifiers

RxCUI
199376 199381
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 (source: ndc)
Generic Name potassium citrate (source: ndc)
Application Number ANDA077440 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 540 mg/1
source: ndc
Packaging
  • 100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (16571-864-01)
source: ndc

Packages (1)

16571-864-01 100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (16571-864-01)

Ingredients (1)

potassium citrate (540 mg/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": "2e4e8acc-d3ad-4246-bd65-d95691896fc8", "openfda": {"unii": ["EE90ONI6FF"], "rxcui": ["199376", "199381"], "spl_set_id": ["164d9d05-fbb1-4d99-8ba3-ff9c172aa8ca"], "manufacturer_name": ["Rising Pharma Holdings, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (16571-864-01)", "package_ndc": "16571-864-01", "marketing_start_date": "20241215"}], "brand_name": "POTASSIUM CITRATE", "product_id": "16571-864_2e4e8acc-d3ad-4246-bd65-d95691896fc8", "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": "16571-864", "generic_name": "potassium citrate", "labeler_name": "Rising Pharma Holdings, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "POTASSIUM CITRATE", "active_ingredients": [{"name": "POTASSIUM CITRATE", "strength": "540 mg/1"}], "application_number": "ANDA077440", "marketing_category": "ANDA", "marketing_start_date": "20241215", "listing_expiration_date": "20271231"}