potassium chloride

Generic: potassium chloride

Labeler: major pharmaceuticals
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name potassium chloride
Generic Name potassium chloride
Labeler major pharmaceuticals
Dosage Form SOLUTION
Routes
ORAL
Active Ingredients

potassium chloride 20 meq/15mL

Manufacturer
Major Pharmaceuticals

Identifiers & Regulatory

Product NDC 0904-7461
Product ID 0904-7461_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
increased large intestinal motility [pe] inhibition large intestine fluid/electrolyte absorption [pe] osmotic activity [moa] osmotic laxative [epc] potassium compounds [cs] potassium salt [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 09047461
Hyphenated Format 0904-7461

Supplemental Identifiers

RxCUI
312515
UPC
0309047461882 0309047462629
UNII
660YQ98I10

Packaging Origin

Original Packager
true

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
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 meq/15mL
source: ndc
Packaging
  • 30 CUP, UNIT-DOSE in 1 CASE (0904-7461-46) / 15 mL in 1 CUP, UNIT-DOSE (0904-7461-88)
  • 80 CUP, UNIT-DOSE in 1 CASE (0904-7461-47) / 15 mL in 1 CUP, UNIT-DOSE (0904-7461-88)
  • 50 CUP, UNIT-DOSE in 1 CASE (0904-7461-51) / 15 mL in 1 CUP, UNIT-DOSE (0904-7461-88)
  • 100 CUP, UNIT-DOSE in 1 CASE (0904-7461-80) / 15 mL in 1 CUP, UNIT-DOSE (0904-7461-88)
  • 40 CUP, UNIT-DOSE in 1 CASE (0904-7461-87) / 15 mL in 1 CUP, UNIT-DOSE (0904-7461-88)
  • 15 mL in 1 CUP, UNIT-DOSE (0904-7461-88)
source: ndc

Packages (6)

Ingredients (1)

potassium chloride (20 meq/15mL)

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": "30 CUP, UNIT-DOSE in 1 CASE (0904-7461-46)  / 15 mL in 1 CUP, UNIT-DOSE (0904-7461-88)", "package_ndc": "0904-7461-46", "marketing_end_date": "20270228", "marketing_start_date": "20240708"}, {"sample": false, "description": "80 CUP, UNIT-DOSE in 1 CASE (0904-7461-47)  / 15 mL in 1 CUP, UNIT-DOSE (0904-7461-88)", "package_ndc": "0904-7461-47", "marketing_end_date": "20261031", "marketing_start_date": "20240711"}, {"sample": false, "description": "50 CUP, UNIT-DOSE in 1 CASE (0904-7461-51)  / 15 mL in 1 CUP, UNIT-DOSE (0904-7461-88)", "package_ndc": "0904-7461-51", "marketing_start_date": "20240708"}, {"sample": false, "description": "100 CUP, UNIT-DOSE in 1 CASE (0904-7461-80)  / 15 mL in 1 CUP, UNIT-DOSE (0904-7461-88)", "package_ndc": "0904-7461-80", "marketing_end_date": "20270228", "marketing_start_date": "20240708"}, {"sample": false, "description": "40 CUP, UNIT-DOSE in 1 CASE (0904-7461-87)  / 15 mL in 1 CUP, UNIT-DOSE (0904-7461-88)", "package_ndc": "0904-7461-87", "marketing_start_date": "20240708"}, {"sample": false, "description": "15 mL in 1 CUP, UNIT-DOSE (0904-7461-88)", "package_ndc": "0904-7461-88", "marketing_start_date": "20240708"}], "brand_name": "POTASSIUM CHLORIDE", "product_id": "0904-7461_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": "0904-7461", "generic_name": "POTASSIUM CHLORIDE", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "POTASSIUM CHLORIDE", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "20 meq/15mL"}], "application_number": "ANDA210766", "marketing_category": "ANDA", "marketing_start_date": "20240708", "listing_expiration_date": "20271231"}