potassium chloride
Generic: potassium chloride
Labeler: endo usa, inc.Drug Facts
Product Profile
Brand Name
potassium chloride
Generic Name
potassium chloride
Labeler
endo usa, inc.
Dosage Form
POWDER, FOR SOLUTION
Routes
Active Ingredients
potassium chloride 1.5 g/1.58g
Manufacturer
Identifiers & Regulatory
Product NDC
0603-1554
Product ID
0603-1554_05260a26-2484-4fd1-9ca1-8445f239923e
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA208019
Listing Expiration
2026-12-31
Marketing Start
2015-09-18
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
06031554
Hyphenated Format
0603-1554
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
- 1.5 g/1.58g
Packaging
- 100 POUCH in 1 CARTON (0603-1554-04) / 1.58 g in 1 POUCH (0603-1554-10)
- 30 POUCH in 1 CARTON (0603-1554-16) / 1.58 g in 1 POUCH (0603-1554-10)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "05260a26-2484-4fd1-9ca1-8445f239923e", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["1867544"], "spl_set_id": ["a64d7151-09a6-474c-83fc-36c7cf582d32"], "manufacturer_name": ["Endo USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 POUCH in 1 CARTON (0603-1554-04) / 1.58 g in 1 POUCH (0603-1554-10)", "package_ndc": "0603-1554-04", "marketing_start_date": "20150918"}, {"sample": false, "description": "30 POUCH in 1 CARTON (0603-1554-16) / 1.58 g in 1 POUCH (0603-1554-10)", "package_ndc": "0603-1554-16", "marketing_start_date": "20150918"}], "brand_name": "Potassium Chloride", "product_id": "0603-1554_05260a26-2484-4fd1-9ca1-8445f239923e", "dosage_form": "POWDER, FOR SOLUTION", "product_ndc": "0603-1554", "generic_name": "Potassium Chloride", "labeler_name": "Endo USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "1.5 g/1.58g"}], "application_number": "NDA208019", "marketing_category": "NDA", "marketing_start_date": "20150918", "listing_expiration_date": "20261231"}