KALI SULPH - 54973-3107-1 - (POTASSIUM SULFATE)

Alphabetical Index


Drug Information of KALI SULPH

Product NDC: 54973-3107
Proprietary Name: KALI SULPH
Non Proprietary Name: POTASSIUM SULFATE
Active Ingredient(s): 30    [hp_X]/1 & nbsp;   POTASSIUM SULFATE
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of KALI SULPH

Product NDC: 54973-3107
Labeler Name: Hyland's
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 19400101

Package Information of KALI SULPH

Package NDC: 54973-3107-1
Package Description: 500 TABLET in 1 BOTTLE, PLASTIC (54973-3107-1)

NDC Information of KALI SULPH

NDC Code 54973-3107-1
Proprietary Name KALI SULPH
Package Description 500 TABLET in 1 BOTTLE, PLASTIC (54973-3107-1)
Product NDC 54973-3107
Product Type Name HUMAN OTC DRUG
Non Proprietary Name POTASSIUM SULFATE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19400101
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name Hyland's
Substance Name POTASSIUM SULFATE
Strength Number 30
Strength Unit [hp_X]/1
Pharmaceutical Classes

Complete Information of KALI SULPH


General Information