NDC 60512-6473

ALNUS GLUTINOSA

Alnus Glutinosa

ALNUS GLUTINOSA is a Oral Pellet in the Human Otc Drug category. It is labeled and distributed by Homeolab Usa Inc.. The primary component is Alnus Glutinosa Bark.

• Product ID: 60512-6473_c159ee04-1389-4ff8-9cd9-e8989fd0ca1f
• NDC: 60512-6473
• Product Type: Human Otc Drug
• Proprietary Name: ALNUS GLUTINOSA
• Generic Name: Alnus Glutinosa
• 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: ALNUS GLUTINOSA BARK
• Active Ingredient Strength: 1 [hp_X]/1
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 60512-6473-1

80 PELLET in 1 TUBE (60512-6473-1)

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

NDC SPL Data Element Entries

NDC 60512-6473-1 [60512647301]

ALNUS GLUTINOSA 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
ALNUS GLUTINOSA BARK	1 [hp_X]/1

OpenFDA Data

• SPL SET ID: ee4825a2-d2c0-402a-9299-823b7824db68
• Manufacturer:
  • HOMEOLAB USA INC.
• UNII:
  • 24A0VB48CA

NDC Crossover Matching brand name "ALNUS GLUTINOSA" or generic name "Alnus Glutinosa"

NDC	Brand Name	Generic Name
15631-0017	ALNUS GLUTINOSA	ALNUS GLUTINOSA
60512-6473	ALNUS GLUTINOSA	ALNUS GLUTINOSA