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 1500 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
71335-1896
Product ID
71335-1896_2f7ac23a-6f65-43f4-9b1e-20b2516e2c3a
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
713351896
Hyphenated Format
71335-1896
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
- 1500 mg/1
Packaging
- 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1896-1)
- 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1896-2)
- 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1896-3)
- 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1896-4)
- 15 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1896-5)
- 7 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1896-6)
- 10 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1896-7)
Packages (7)
71335-1896-1
30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1896-1)
71335-1896-2
60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1896-2)
71335-1896-3
100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1896-3)
71335-1896-4
90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1896-4)
71335-1896-5
15 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1896-5)
71335-1896-6
7 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1896-6)
71335-1896-7
10 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1896-7)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2f7ac23a-6f65-43f4-9b1e-20b2516e2c3a", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["1801294"], "spl_set_id": ["7b8e7a4f-0d44-46b2-9565-7b4c294e9fcb"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1896-1)", "package_ndc": "71335-1896-1", "marketing_start_date": "20240718"}, {"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1896-2)", "package_ndc": "71335-1896-2", "marketing_start_date": "20210902"}, {"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1896-3)", "package_ndc": "71335-1896-3", "marketing_start_date": "20240718"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1896-4)", "package_ndc": "71335-1896-4", "marketing_start_date": "20210622"}, {"sample": false, "description": "15 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1896-5)", "package_ndc": "71335-1896-5", "marketing_start_date": "20240718"}, {"sample": false, "description": "7 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1896-6)", "package_ndc": "71335-1896-6", "marketing_start_date": "20240718"}, {"sample": false, "description": "10 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1896-7)", "package_ndc": "71335-1896-7", "marketing_start_date": "20240718"}], "brand_name": "Potassium Chloride Extended-release", "product_id": "71335-1896_2f7ac23a-6f65-43f4-9b1e-20b2516e2c3a", "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": "71335-1896", "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": "1500 mg/1"}], "application_number": "ANDA214452", "marketing_category": "ANDA", "marketing_start_date": "20210130", "listing_expiration_date": "20261231"}