NDC 60512-6176

AMMONIUM VALERIANICUM

Ammonium Valerianicum

AMMONIUM VALERIANICUM is a Oral Pellet in the Human Otc Drug category. It is labeled and distributed by Homeolab Usa Inc.. The primary component is Ammonium Valerate.

• Product ID: 60512-6176_de300e22-fcd8-4c97-917e-d04682f0bc75
• NDC: 60512-6176
• Product Type: Human Otc Drug
• Proprietary Name: AMMONIUM VALERIANICUM
• Generic Name: Ammonium Valerianicum
• 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: AMMONIUM VALERATE
• Active Ingredient Strength: 2 [hp_X]/1
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 60512-6176-1

80 PELLET in 1 TUBE (60512-6176-1)

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

NDC SPL Data Element Entries

NDC 60512-6176-1 [60512617601]

AMMONIUM VALERIANICUM 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
AMMONIUM VALERATE	2 [hp_X]/1

OpenFDA Data

• SPL SET ID: ce3a792e-2db3-4002-a912-a5eefdce9332
• Manufacturer:
  • HOMEOLAB USA INC.
• UNII:
  • 0U3170A41K

NDC Crossover Matching brand name "AMMONIUM VALERIANICUM" or generic name "Ammonium Valerianicum"

NDC	Brand Name	Generic Name
60512-6176	AMMONIUM VALERIANICUM	AMMONIUM VALERIANICUM
68428-880	Ammonium valerianicum	AMMONIUM VALERATE
71919-048	Ammonium valerianicum	AMMONIUM VALERATE