NDC 63545-688

Vanilla Planifolia

Vanilla Planifolia

Vanilla Planifolia is a Buccal; Oral; Sublingual Pellet in the Human Otc Drug category. It is labeled and distributed by Hahnemann Laboratories, Inc.. The primary component is Vanilla Planifolia Whole.

• Product ID: 63545-688_4ec9b6dd-d634-3cc1-e054-00144ff88e88
• NDC: 63545-688
• Product Type: Human Otc Drug
• Proprietary Name: Vanilla Planifolia
• Generic Name: Vanilla Planifolia
• Dosage Form: Pellet
• Route of Administration: BUCCAL; ORAL; SUBLINGUAL
• Marketing Start Date: 2017-05-05
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Hahnemann Laboratories, Inc.
• Substance Name: VANILLA PLANIFOLIA WHOLE
• Active Ingredient Strength: 30 [hp_C]/[hp_C]
• NDC Exclude Flag: E
• Listing Certified Through: 2018-12-31

Packaging

NDC 63545-688-01

240 [hp_C] in 1 VIAL, GLASS (63545-688-01)

• Marketing Start Date: 2017-05-05
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 63545-688-01 [63545068801]

Vanilla Planifolia PELLET

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2017-05-05
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
VANILLA PLANIFOLIA WHOLE	30 [hp_C]/[hp_C]

OpenFDA Data

• SPL SET ID: 4ec9b6dd-d633-3cc1-e054-00144ff88e88
• Manufacturer:
  • Hahnemann Laboratories, Inc.
• UNII:
  • BOS0R5Y21O

NDC Crossover Matching brand name "Vanilla Planifolia" or generic name "Vanilla Planifolia"

NDC	Brand Name	Generic Name
63545-688	Vanilla Planifolia	Vanilla Planifolia
0268-6230	VANILLA	VANILLA PLANIFOLIA
22840-5754	Vanilla	Vanilla planifolia