PHOSPHORUS - 54973-0622-4 - (PHOSPHORUS)

Alphabetical Index


Drug Information of PHOSPHORUS

Product NDC: 54973-0622
Proprietary Name: PHOSPHORUS
Non Proprietary Name: PHOSPHORUS
Active Ingredient(s): 6    [hp_X]/1 & nbsp;   PHOSPHORUS
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of PHOSPHORUS

Product NDC: 54973-0622
Labeler Name: Hyland's
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 19550101

Package Information of PHOSPHORUS

Package NDC: 54973-0622-4
Package Description: 250 TABLET in 1 BOTTLE, PLASTIC (54973-0622-4)

NDC Information of PHOSPHORUS

NDC Code 54973-0622-4
Proprietary Name PHOSPHORUS
Package Description 250 TABLET in 1 BOTTLE, PLASTIC (54973-0622-4)
Product NDC 54973-0622
Product Type Name HUMAN OTC DRUG
Non Proprietary Name PHOSPHORUS
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19550101
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name Hyland's
Substance Name PHOSPHORUS
Strength Number 6
Strength Unit [hp_X]/1
Pharmaceutical Classes

Complete Information of PHOSPHORUS


General Information