potassium citrate extended release

Generic: potassium citrate

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name potassium citrate extended release
Generic Name potassium citrate
Labeler bryant ranch prepack
Dosage Form TABLET
Routes
ORAL
Active Ingredients

potassium citrate 10 meq/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-1706
Product ID 71335-1706_8212127c-30d8-41f6-9f2b-ddeed4c6ad1a
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 713351706
Hyphenated Format 71335-1706

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 extended release (source: ndc)
Generic Name potassium citrate (source: ndc)
Application Number ANDA206813 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 meq/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (71335-1706-1)
source: ndc

Packages (1)

71335-1706-1 30 TABLET in 1 BOTTLE (71335-1706-1)

Ingredients (1)

potassium citrate (10 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": "8212127c-30d8-41f6-9f2b-ddeed4c6ad1a", "openfda": {"unii": ["EE90ONI6FF"], "rxcui": ["199381"], "spl_set_id": ["9774b7c5-4695-47c9-9eb8-e0af2e05f5c3"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-1706-1)", "package_ndc": "71335-1706-1", "marketing_start_date": "20200910"}], "brand_name": "POTASSIUM CITRATE EXTENDED RELEASE", "product_id": "71335-1706_8212127c-30d8-41f6-9f2b-ddeed4c6ad1a", "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": "71335-1706", "generic_name": "POTASSIUM CITRATE", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "POTASSIUM CITRATE", "brand_name_suffix": "EXTENDED RELEASE", "active_ingredients": [{"name": "POTASSIUM CITRATE", "strength": "10 meq/1"}], "application_number": "ANDA206813", "marketing_category": "ANDA", "marketing_start_date": "20171101", "listing_expiration_date": "20261231"}