potassium citrate

Generic: potassium citrate

Labeler: american health packaging
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name potassium citrate
Generic Name potassium citrate
Labeler american health packaging
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

potassium citrate 10 meq/1

Manufacturer
American Health Packaging

Identifiers & Regulatory

Product NDC 68084-850
Product ID 68084-850_213c9f49-5d37-f84f-e063-6394a90aa698
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203546
Listing Expiration 2026-12-31
Marketing Start 2014-11-12

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 68084850
Hyphenated Format 68084-850

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 ANDA203546 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 meq/1
source: ndc
Packaging
  • 20 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-850-32) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (68084-850-33)
source: ndc

Packages (1)

68084-850-32 20 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-850-32) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (68084-850-33)

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": "213c9f49-5d37-f84f-e063-6394a90aa698", "openfda": {"unii": ["EE90ONI6FF"], "rxcui": ["199381"], "spl_set_id": ["1201c777-2388-4235-bb8f-eb7dc1e867f8"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "20 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-850-32)  / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (68084-850-33)", "package_ndc": "68084-850-32", "marketing_start_date": "20141112"}], "brand_name": "Potassium Citrate", "product_id": "68084-850_213c9f49-5d37-f84f-e063-6394a90aa698", "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": "68084-850", "generic_name": "Potassium Citrate", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Citrate", "active_ingredients": [{"name": "POTASSIUM CITRATE", "strength": "10 meq/1"}], "application_number": "ANDA203546", "marketing_category": "ANDA", "marketing_start_date": "20141112", "listing_expiration_date": "20261231"}