potassium citrate

Generic: potassium citrate

Labeler: ani pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

potassium citrate 10 meq/1

Manufacturer
ANI Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 62559-291
Product ID 62559-291_ce0ee9e0-f0bc-4578-b4cd-d3d353171e82
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA212779
Listing Expiration 2026-12-31
Marketing Start 2020-03-16

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 62559291
Hyphenated Format 62559-291

Supplemental Identifiers

RxCUI
199381 898490
UPC
0362559291019 0362559292016
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 ANDA212779 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 meq/1
source: ndc
Packaging
  • 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (62559-291-01)
source: ndc

Packages (1)

62559-291-01 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (62559-291-01)

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": "ce0ee9e0-f0bc-4578-b4cd-d3d353171e82", "openfda": {"upc": ["0362559291019", "0362559292016"], "unii": ["EE90ONI6FF"], "rxcui": ["199381", "898490"], "spl_set_id": ["2fb31727-68b1-4183-947d-00e08bf99987"], "manufacturer_name": ["ANI Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (62559-291-01)", "package_ndc": "62559-291-01", "marketing_start_date": "20200316"}], "brand_name": "Potassium Citrate", "product_id": "62559-291_ce0ee9e0-f0bc-4578-b4cd-d3d353171e82", "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": "62559-291", "generic_name": "Potassium Citrate", "labeler_name": "ANI Pharmaceuticals, Inc.", "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"}