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 ID: 60512-6439_f9cce9a3-dd8b-405b-98aa-2cd91784f5dc
• NDC: 60512-6439
• Product Type: Human Otc Drug
• Proprietary Name: ABSINTHIUM
• Generic Name: Absinthium
• Dosage Form: Pellet
• Route of Administration: ORAL
• Marketing Start Date: 1995-10-11
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: HOMEOLAB USA INC.
• Substance Name: ARTEMISIA ABSINTHIUM WHOLE
• Active Ingredient Strength: 3 [hp_X]/1
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 60512-6439-1

80 PELLET in 1 TUBE (60512-6439-1)

• Marketing Start Date: 1995-10-11
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 60512-6439-1 [60512643901]

ABSINTHIUM PELLET

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 1995-10-11
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
ARTEMISIA ABSINTHIUM WHOLE	3 [hp_X]/1

OpenFDA Data

• SPL SET ID: 3e361090-9d25-4a15-bf66-08d7a98924fa
• Manufacturer:
  • HOMEOLAB USA INC.
• UNII:
  • 51PW3BIW1K

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

NDC	Brand Name	Generic Name
0220-0018	Absinthium	WORMWOOD
15631-0003	ABSINTHIUM	ABSINTHIUM
60512-6439	ABSINTHIUM	ABSINTHIUM
63545-258	Absinthium	Absinthium
63545-717	Absinthium	Absinthium
63545-718	Absinthium	Absinthium
63545-719	Absinthium	Absinthium
63545-720	Absinthium	Absinthium
63545-721	Absinthium	Absinthium
63545-722	Absinthium	Absinthium
68428-174	Absinthium	Absinthium
71919-004	Absinthium	Absinthium
63545-723	Absinthium	Absinthium