NDC 69152-1015

Cantharis 200C

Cantharis

Cantharis 200C is a Oral Pellet in the Human Otc Drug category. It is labeled and distributed by Paramesh Banerji Life Sciences Llc. The primary component is Lytta Vesicatoria.

• Product ID: 69152-1015_2f2e2220-6fca-0e0a-e054-00144ff8d46c
• NDC: 69152-1015
• Product Type: Human Otc Drug
• Proprietary Name: Cantharis 200C
• Generic Name: Cantharis
• Dosage Form: Pellet
• Route of Administration: ORAL
• Marketing Start Date: 2015-05-21
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Paramesh Banerji Life Sciences LLC
• Substance Name: LYTTA VESICATORIA
• Active Ingredient Strength: 200 [hp_C]/1
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 69152-1015-1

96 PELLET in 1 BOTTLE (69152-1015-1)

• Marketing Start Date: 2015-05-21
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 69152-1015-1 [69152101501]

Cantharis 200C PELLET

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2015-05-21
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
LYTTA VESICATORIA	200 [hp_C]/1

OpenFDA Data

• SPL SET ID: 169508a6-4dc9-39f5-e054-00144ff88e88
• Manufacturer:
  • Paramesh Banerji Life Sciences LLC
• UNII:
  • 3Q034RO3BT

NDC Crossover Matching brand name "Cantharis 200C" or generic name "Cantharis"

NDC	Brand Name	Generic Name
69152-1015	Cantharis 200C	Cantharis
0360-0093	CANTHARIS	CANTHARIS
0360-0094	CANTHARIS	CANTHARIS
15631-0105	CANTHARIS	CANTHARIS
15631-0552	CANTHARIS	CANTHARIS
15631-2311	CANTHARIS	CANTHARIS
53645-1660	Cantharis	Cantharis
60512-9151	CANTHARIS	CANTHARIS
63083-7111	Cantharis	Cantharis
69152-1213	Cantharis 6C	Cantharis