potassium chloride
Generic: potassium chloride
Labeler: major pharmaceuticalsDrug Facts
Product Profile
Brand Name
potassium chloride
Generic Name
potassium chloride
Labeler
major pharmaceuticals
Dosage Form
SOLUTION
Routes
Active Ingredients
potassium chloride 40 meq/30mL
Manufacturer
Identifiers & Regulatory
Product NDC
0904-7462
Product ID
0904-7462_0e0defca-901d-4b4b-ac96-ac72fcfe4303
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA210766
Listing Expiration
2027-12-31
Marketing Start
2024-07-08
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
09047462
Hyphenated Format
0904-7462
Supplemental Identifiers
RxCUI
UPC
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
ANDA210766 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 40 meq/30mL
Packaging
- 50 CUP, UNIT-DOSE in 1 CASE (0904-7462-43) / 30 mL in 1 CUP, UNIT-DOSE (0904-7462-62)
- 40 CUP, UNIT-DOSE in 1 CASE (0904-7462-60) / 30 mL in 1 CUP, UNIT-DOSE (0904-7462-62)
- 30 mL in 1 CUP, UNIT-DOSE (0904-7462-62)
- 100 CUP, UNIT-DOSE in 1 CASE (0904-7462-73) / 30 mL in 1 CUP, UNIT-DOSE (0904-7462-62)
Packages (4)
0904-7462-43
50 CUP, UNIT-DOSE in 1 CASE (0904-7462-43) / 30 mL in 1 CUP, UNIT-DOSE (0904-7462-62)
0904-7462-60
40 CUP, UNIT-DOSE in 1 CASE (0904-7462-60) / 30 mL in 1 CUP, UNIT-DOSE (0904-7462-62)
0904-7462-62
30 mL in 1 CUP, UNIT-DOSE (0904-7462-62)
0904-7462-73
100 CUP, UNIT-DOSE in 1 CASE (0904-7462-73) / 30 mL in 1 CUP, UNIT-DOSE (0904-7462-62)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0e0defca-901d-4b4b-ac96-ac72fcfe4303", "openfda": {"upc": ["0309047461882", "0309047462629"], "unii": ["660YQ98I10"], "rxcui": ["312515"], "spl_set_id": ["33ad1eb2-1f05-461c-b01d-82dee4231556"], "manufacturer_name": ["Major Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 CUP, UNIT-DOSE in 1 CASE (0904-7462-43) / 30 mL in 1 CUP, UNIT-DOSE (0904-7462-62)", "package_ndc": "0904-7462-43", "marketing_end_date": "20270531", "marketing_start_date": "20240708"}, {"sample": false, "description": "40 CUP, UNIT-DOSE in 1 CASE (0904-7462-60) / 30 mL in 1 CUP, UNIT-DOSE (0904-7462-62)", "package_ndc": "0904-7462-60", "marketing_start_date": "20240708"}, {"sample": false, "description": "30 mL in 1 CUP, UNIT-DOSE (0904-7462-62)", "package_ndc": "0904-7462-62", "marketing_start_date": "20240708"}, {"sample": false, "description": "100 CUP, UNIT-DOSE in 1 CASE (0904-7462-73) / 30 mL in 1 CUP, UNIT-DOSE (0904-7462-62)", "package_ndc": "0904-7462-73", "marketing_start_date": "20240708"}], "brand_name": "POTASSIUM CHLORIDE", "product_id": "0904-7462_0e0defca-901d-4b4b-ac96-ac72fcfe4303", "dosage_form": "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": "0904-7462", "generic_name": "POTASSIUM CHLORIDE", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "POTASSIUM CHLORIDE", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "40 meq/30mL"}], "application_number": "ANDA210766", "marketing_category": "ANDA", "marketing_start_date": "20240708", "listing_expiration_date": "20271231"}