NDC 60512-6447

ADONIS VERNALIS

Adonis Vernalis

ADONIS VERNALIS is a Oral Pellet in the Human Otc Drug category. It is labeled and distributed by Homeolab Usa Inc.. The primary component is Adonis Vernalis.

• Product ID: 60512-6447_2002e89d-bceb-43e8-8107-b441358926eb
• NDC: 60512-6447
• Product Type: Human Otc Drug
• Proprietary Name: ADONIS VERNALIS
• Generic Name: Adonis Vernalis
• 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: ADONIS VERNALIS
• Active Ingredient Strength: 3 [hp_X]/1
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 60512-6447-1

80 PELLET in 1 TUBE (60512-6447-1)

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

NDC SPL Data Element Entries

NDC 60512-6447-1 [60512644701]

ADONIS VERNALIS 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
ADONIS VERNALIS	3 [hp_X]/1

OpenFDA Data

• SPL SET ID: b9b20ccc-d05d-4ede-9f34-097988fcf3f9
• Manufacturer:
  • HOMEOLAB USA INC.
• UNII:
  • DX3ZNI25WK

NDC Crossover Matching brand name "ADONIS VERNALIS" or generic name "Adonis Vernalis"

NDC	Brand Name	Generic Name
60512-6447	ADONIS VERNALIS	ADONIS VERNALIS
68428-179	Adonis vernalis	ADONIS VERNALIS
71919-013	Adonis vernalis	ADONIS VERNALIS
71919-049	Ampelopsis quinquefolia	ADONIS VERNALIS
64117-301	NHS HEADACHE	ADONIS VERNALIS