NDC 68382-701 Potassium Chloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 68382 - Zydus Pharmaceuticals (usa) Inc.
- 68382-701 - Potassium Chloride
Product Characteristics
WHITE (C48325 - OPAQUE WHITE)
001;001
Product Packages
NDC Code 68382-701-01
Package Description: 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE
Price per Unit: $0.18327 per EA
NDC Code 68382-701-05
Package Description: 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE
Price per Unit: $0.18327 per EA
Product Details
What is NDC 68382-701?
What are the uses for Potassium Chloride?
Which are Potassium Chloride UNII Codes?
The UNII codes for the active ingredients in this product are:
- POTASSIUM CHLORIDE (UNII: 660YQ98I10)
- POTASSIUM CATION (UNII: 295O53K152) (Active Moiety)
Which are Potassium Chloride Inactive Ingredients UNII Codes?
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:
- ETHYLCELLULOSES (UNII: 7Z8S9VYZ4B)
- FD&C BLUE NO. 2 (UNII: L06K8R7DQK)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
- GELATIN (UNII: 2G86QN327L)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- ALUMINUM OXIDE (UNII: LMI26O6933)
What is the NDC to RxNorm Crosswalk for Potassium Chloride?
- RxCUI: 312504 - potassium chloride 10 MEQ Extended Release Oral Capsule
- RxCUI: 312504 - K+ Chloride 10 MEQ Extended Release Oral Capsule
- RxCUI: 312504 - Pot Chloride 10 MEQ Extended Release Oral Capsule
- RxCUI: 312504 - potassium chloride 750 MG Extended Release Oral Capsule
- RxCUI: 315183 - potassium chloride 8 MEQ (600 MG) Extended Release Oral Capsule
* Please review the disclaimer below.
Patient Education
Potassium
Potassium is essential for the proper functioning of the heart, kidneys, muscles, nerves, and digestive system. Usually the food you eat supplies all of the potassium you need. However, certain diseases (e.g., kidney disease and gastrointestinal disease with vomiting and diarrhea) and drugs, especially diuretics ('water pills'), remove potassium from the body. Potassium supplements are taken to replace potassium losses and prevent potassium deficiency. This medication is sometimes prescribed for other uses; ask your doctor or pharmacist for more information.
[Learn More]
* Please review the disclaimer below.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.
[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".