potassium chloride
Generic: potassium chloride
Labeler: bryant ranch prepackDrug Facts
Product Profile
Brand Name
potassium chloride
Generic Name
potassium chloride
Labeler
bryant ranch prepack
Dosage Form
TABLET, EXTENDED RELEASE
Routes
Active Ingredients
potassium chloride 750 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
71335-1781
Product ID
71335-1781_9ab3989d-07c9-44d3-b84b-a7b1405d17db
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA203562
Listing Expiration
2026-12-31
Marketing Start
2016-07-26
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
713351781
Hyphenated Format
71335-1781
Supplemental Identifiers
RxCUI
UNII
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 chloride (source: ndc)
Generic Name
potassium chloride (source: ndc)
Application Number
ANDA203562 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 750 mg/1
Packaging
- 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1781-1)
- 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1781-2)
- 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1781-3)
- 15 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1781-4)
- 180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1781-5)
- 28 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1781-6)
- 10 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1781-7)
Packages (7)
71335-1781-1
30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1781-1)
71335-1781-2
60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1781-2)
71335-1781-3
90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1781-3)
71335-1781-4
15 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1781-4)
71335-1781-5
180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1781-5)
71335-1781-6
28 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1781-6)
71335-1781-7
10 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1781-7)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "9ab3989d-07c9-44d3-b84b-a7b1405d17db", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["1801298"], "spl_set_id": ["bc42a691-a486-4ece-b9f7-faf6cc5df6b5"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1781-1)", "package_ndc": "71335-1781-1", "marketing_start_date": "20210526"}, {"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1781-2)", "package_ndc": "71335-1781-2", "marketing_start_date": "20210625"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1781-3)", "package_ndc": "71335-1781-3", "marketing_start_date": "20210309"}, {"sample": false, "description": "15 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1781-4)", "package_ndc": "71335-1781-4", "marketing_start_date": "20211220"}, {"sample": false, "description": "180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1781-5)", "package_ndc": "71335-1781-5", "marketing_start_date": "20211220"}, {"sample": false, "description": "28 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1781-6)", "package_ndc": "71335-1781-6", "marketing_start_date": "20211220"}, {"sample": false, "description": "10 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1781-7)", "package_ndc": "71335-1781-7", "marketing_start_date": "20210308"}], "brand_name": "potassium chloride", "product_id": "71335-1781_9ab3989d-07c9-44d3-b84b-a7b1405d17db", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Increased Large Intestinal Motility [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]", "Potassium Compounds [CS]", "Potassium Salt [EPC]"], "product_ndc": "71335-1781", "generic_name": "potassium chloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "potassium chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "750 mg/1"}], "application_number": "ANDA203562", "marketing_category": "ANDA", "marketing_start_date": "20160726", "listing_expiration_date": "20261231"}