NDC 60512-6468

ALETRIS FARINOSA

Aletris Farinosa

ALETRIS FARINOSA is a Oral Pellet in the Human Otc Drug category. It is labeled and distributed by Homeolab Usa Inc.. The primary component is Aletris Farinosa Root.

• Product ID: 60512-6468_e9917566-8144-4222-9409-308b09ebd5ca
• NDC: 60512-6468
• Product Type: Human Otc Drug
• Proprietary Name: ALETRIS FARINOSA
• Generic Name: Aletris Farinosa
• 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: ALETRIS FARINOSA ROOT
• Active Ingredient Strength: 1 [hp_X]/1
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 60512-6468-1

80 PELLET in 1 TUBE (60512-6468-1)

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

NDC SPL Data Element Entries

NDC 60512-6468-1 [60512646801]

ALETRIS FARINOSA 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
ALETRIS FARINOSA ROOT	1 [hp_X]/1

OpenFDA Data

• SPL SET ID: 43ee58a3-cd93-40dd-94ce-4217e6e1a5fd
• Manufacturer:
  • HOMEOLAB USA INC.
• UNII:
  • O021JGR97X

NDC Crossover Matching brand name "ALETRIS FARINOSA" or generic name "Aletris Farinosa"

NDC	Brand Name	Generic Name
0220-0160	Aletris farinosa	ALETRIS FARINOSA ROOT
15631-0013	ALETRIS FARINOSA	ALETRIS FARINOSA
60512-6468	ALETRIS FARINOSA	ALETRIS FARINOSA
68428-187	Aletris farinosa	ALETRIS FARINOSA ROOT
71919-026	Aletris farinosa	ALETRIS FARINOSA ROOT