NDC 60512-6439

ABSINTHIUM

Absinthium

ABSINTHIUM is a Oral Pellet in the Human Otc Drug category. It is labeled and distributed by Homeolab Usa Inc.. The primary component is Artemisia Absinthium Whole.

Product ID60512-6439_f9cce9a3-dd8b-405b-98aa-2cd91784f5dc
NDC60512-6439
Product TypeHuman Otc Drug
Proprietary NameABSINTHIUM
Generic NameAbsinthium
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date1995-10-11
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameHOMEOLAB USA INC.
Substance NameARTEMISIA ABSINTHIUM WHOLE
Active Ingredient Strength3 [hp_X]/1
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 60512-6439-1

80 PELLET in 1 TUBE (60512-6439-1)
Marketing Start Date1995-10-11
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 60512-6439-1 [60512643901]

ABSINTHIUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date1995-10-11
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
ARTEMISIA ABSINTHIUM WHOLE3 [hp_X]/1

OpenFDA Data

SPL SET ID:3e361090-9d25-4a15-bf66-08d7a98924fa
Manufacturer
UNII

NDC Crossover Matching brand name "ABSINTHIUM" or generic name "Absinthium"

NDCBrand NameGeneric Name
0220-0018AbsinthiumWORMWOOD
15631-0003ABSINTHIUMABSINTHIUM
60512-6439ABSINTHIUMABSINTHIUM
63545-258AbsinthiumAbsinthium
63545-717AbsinthiumAbsinthium
63545-718AbsinthiumAbsinthium
63545-719AbsinthiumAbsinthium
63545-720AbsinthiumAbsinthium
63545-721AbsinthiumAbsinthium
63545-722AbsinthiumAbsinthium
68428-174AbsinthiumAbsinthium
71919-004AbsinthiumAbsinthium
63545-723AbsinthiumAbsinthium

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