Hevert - 54532-0012-4 - (APIS MELLIFERA, GALPHIMIA GLAUCA WHOLE, POTASSIUM DICHROMATE, TEUCRIUM MARUM TOP, and VERBASCUM DENSIFLORUM FLOWERING TOP)

Alphabetical Index


Drug Information of Hevert

Product NDC: 54532-0012
Proprietary Name: Hevert
Non Proprietary Name: APIS MELLIFERA, GALPHIMIA GLAUCA WHOLE, POTASSIUM DICHROMATE, TEUCRIUM MARUM TOP, and VERBASCUM DENSIFLORUM FLOWERING TOP
Active Ingredient(s): 4; 4; 6; 4; 2    [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1 & nbsp;   APIS MELLIFERA, GALPHIMIA GLAUCA WHOLE, POTASSIUM DICHROMATE, TEUCRIUM MARUM TOP, and VERBASCUM DENSIFLORUM FLOWERING TOP
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Hevert

Product NDC: 54532-0012
Labeler Name: Hevert Pharmaceuticals LLC
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 20130201

Package Information of Hevert

Package NDC: 54532-0012-4
Package Description: 10 BLISTER PACK in 1 CARTON (54532-0012-4) > 10 TABLET in 1 BLISTER PACK

NDC Information of Hevert

NDC Code 54532-0012-4
Proprietary Name Hevert
Package Description 10 BLISTER PACK in 1 CARTON (54532-0012-4) > 10 TABLET in 1 BLISTER PACK
Product NDC 54532-0012
Product Type Name HUMAN OTC DRUG
Non Proprietary Name APIS MELLIFERA, GALPHIMIA GLAUCA WHOLE, POTASSIUM DICHROMATE, TEUCRIUM MARUM TOP, and VERBASCUM DENSIFLORUM FLOWERING TOP
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130201
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name Hevert Pharmaceuticals LLC
Substance Name APIS MELLIFERA; GALPHIMIA GLAUCA WHOLE; POTASSIUM DICHROMATE; TEUCRIUM MARUM TOP; VERBASCUM DENSIFLORUM FLOWERING TOP
Strength Number 4; 4; 6; 4; 2
Strength Unit [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1
Pharmaceutical Classes

Complete Information of Hevert


General Information