BELLADONNA - 60512-1006-1 - (BELLADONNA)

Alphabetical Index


Drug Information of BELLADONNA

Product NDC: 60512-1006
Proprietary Name: BELLADONNA
Non Proprietary Name: BELLADONNA
Active Ingredient(s): 3    [hp_X]/1 & nbsp;   BELLADONNA
Administration Route(s): ORAL
Dosage Form(s): PELLET
Coding System: National Drug Codes(NDC)

Labeler Information of BELLADONNA

Product NDC: 60512-1006
Labeler Name: HOMEOLAB USA INC
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 19951011

Package Information of BELLADONNA

Package NDC: 60512-1006-1
Package Description: 80 PELLET in 1 TUBE (60512-1006-1)

NDC Information of BELLADONNA

NDC Code 60512-1006-1
Proprietary Name BELLADONNA
Package Description 80 PELLET in 1 TUBE (60512-1006-1)
Product NDC 60512-1006
Product Type Name HUMAN OTC DRUG
Non Proprietary Name BELLADONNA
Dosage Form Name PELLET
Route Name ORAL
Start Marketing Date 19951011
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name HOMEOLAB USA INC
Substance Name ATROPA BELLADONNA
Strength Number 3
Strength Unit [hp_X]/1
Pharmaceutical Classes

Complete Information of BELLADONNA


General Information