potassium chloride
Generic: potassium chloride
Labeler: ipg pharmaceuticals, inc.Drug Facts
Product Profile
Brand Name
potassium chloride
Generic Name
potassium chloride
Labeler
ipg pharmaceuticals, inc.
Dosage Form
FOR SOLUTION
Routes
Active Ingredients
potassium chloride 3 g/3.16g
Manufacturer
Identifiers & Regulatory
Product NDC
71085-083
Product ID
71085-083_dc4ae7ec-789f-4f7e-8a85-c99f3586dabe
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA208019
Listing Expiration
2026-12-31
Marketing Start
2025-12-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
71085083
Hyphenated Format
71085-083
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
NDA208019 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 3 g/3.16g
Packaging
- 30 POUCH in 1 CARTON (71085-083-30) / 3.16 g in 1 POUCH (71085-083-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "dc4ae7ec-789f-4f7e-8a85-c99f3586dabe", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["2728724"], "spl_set_id": ["5dad0879-0f97-4c7d-98fa-baaed51cd2d8"], "manufacturer_name": ["IPG Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 POUCH in 1 CARTON (71085-083-30) / 3.16 g in 1 POUCH (71085-083-01)", "package_ndc": "71085-083-30", "marketing_start_date": "20251201"}], "brand_name": "Potassium Chloride", "product_id": "71085-083_dc4ae7ec-789f-4f7e-8a85-c99f3586dabe", "dosage_form": "FOR SOLUTION", "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": "71085-083", "generic_name": "Potassium Chloride", "labeler_name": "IPG Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "3 g/3.16g"}], "application_number": "NDA208019", "marketing_category": "NDA", "marketing_start_date": "20251201", "listing_expiration_date": "20261231"}