potassium chloride extended-release
Generic: potassium chloride extended-release
Labeler: bryant ranch prepackDrug Facts
Product Profile
Brand Name
potassium chloride extended-release
Generic Name
potassium chloride extended-release
Labeler
bryant ranch prepack
Dosage Form
TABLET, EXTENDED RELEASE
Routes
Active Ingredients
potassium chloride 750 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
71335-2503
Product ID
71335-2503_541c34f6-fee2-4878-ac6c-5a46ac3be59d
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA214452
Listing Expiration
2026-12-31
Marketing Start
2021-01-30
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
713352503
Hyphenated Format
71335-2503
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 extended-release (source: ndc)
Generic Name
potassium chloride extended-release (source: ndc)
Application Number
ANDA214452 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 750 mg/1
Packaging
- 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2503-1)
- 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2503-2)
- 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2503-3)
- 15 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2503-4)
- 180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2503-5)
- 28 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2503-6)
- 10 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2503-7)
Packages (7)
71335-2503-1
30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2503-1)
71335-2503-2
60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2503-2)
71335-2503-3
90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2503-3)
71335-2503-4
15 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2503-4)
71335-2503-5
180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2503-5)
71335-2503-6
28 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2503-6)
71335-2503-7
10 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2503-7)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "541c34f6-fee2-4878-ac6c-5a46ac3be59d", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["1801298"], "spl_set_id": ["b5505a39-57f1-4ed5-b845-4f1d8aa10950"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2503-1)", "package_ndc": "71335-2503-1", "marketing_start_date": "20240923"}, {"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2503-2)", "package_ndc": "71335-2503-2", "marketing_start_date": "20240923"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2503-3)", "package_ndc": "71335-2503-3", "marketing_start_date": "20240923"}, {"sample": false, "description": "15 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2503-4)", "package_ndc": "71335-2503-4", "marketing_start_date": "20240923"}, {"sample": false, "description": "180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2503-5)", "package_ndc": "71335-2503-5", "marketing_start_date": "20240923"}, {"sample": false, "description": "28 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2503-6)", "package_ndc": "71335-2503-6", "marketing_start_date": "20240923"}, {"sample": false, "description": "10 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2503-7)", "package_ndc": "71335-2503-7", "marketing_start_date": "20240923"}], "brand_name": "Potassium Chloride Extended-release", "product_id": "71335-2503_541c34f6-fee2-4878-ac6c-5a46ac3be59d", "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": "71335-2503", "generic_name": "Potassium Chloride Extended-release", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride Extended-release", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "750 mg/1"}], "application_number": "ANDA214452", "marketing_category": "ANDA", "marketing_start_date": "20210130", "listing_expiration_date": "20261231"}