Package 71335-1706-1

Brand: potassium citrate extended release

Generic: potassium citrate
NDC Package

Package Facts

Identity

Package NDC 71335-1706-1
Digits Only 7133517061
Product NDC 71335-1706
Product ID 71335-1706_8212127c-30d8-41f6-9f2b-ddeed4c6ad1a
Description

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

Marketing

Marketing Status
Marketed Since 2020-09-10
Brand potassium citrate extended release
Generic potassium citrate
Sample Package No

Linked Drug Pages (1)

POTASSIUM CITRATE EXTENDED RELEASE ndc-match (0.95)

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"}