NAT SULPH - 54973-3111-2 - (SODIUM SULFATE ANHYDROUS)

Alphabetical Index


Drug Information of NAT SULPH

Product NDC: 54973-3111
Proprietary Name: NAT SULPH
Non Proprietary Name: SODIUM SULFATE ANHYDROUS
Active Ingredient(s): 30    [hp_X]/1 & nbsp;   SODIUM SULFATE ANHYDROUS
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of NAT SULPH

Product NDC: 54973-3111
Labeler Name: Hyland's
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 19400101

Package Information of NAT SULPH

Package NDC: 54973-3111-2
Package Description: 1000 TABLET in 1 BOTTLE, PLASTIC (54973-3111-2)

NDC Information of NAT SULPH

NDC Code 54973-3111-2
Proprietary Name NAT SULPH
Package Description 1000 TABLET in 1 BOTTLE, PLASTIC (54973-3111-2)
Product NDC 54973-3111
Product Type Name HUMAN OTC DRUG
Non Proprietary Name SODIUM SULFATE ANHYDROUS
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19400101
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name Hyland's
Substance Name SODIUM SULFATE ANHYDROUS
Strength Number 30
Strength Unit [hp_X]/1
Pharmaceutical Classes

Complete Information of NAT SULPH


General Information