NDC 0360-0139

COCCULUS

Cocculus Ind.

COCCULUS is a Sublingual Tablet in the Human Otc Drug category. It is labeled and distributed by Standard Homeopathic Company. The primary component is Anamirta Cocculus Seed.

• Product ID: 0360-0139_7c22c499-d819-6c0f-e053-2991aa0a9931
• NDC: 0360-0139
• Product Type: Human Otc Drug
• Proprietary Name: COCCULUS
• Generic Name: Cocculus Ind.
• Dosage Form: Tablet
• Route of Administration: SUBLINGUAL
• Marketing Start Date: 1997-02-17
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: STANDARD HOMEOPATHIC COMPANY
• Substance Name: ANAMIRTA COCCULUS SEED
• Active Ingredient Strength: 6 [hp_X]/g
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 0360-0139-01

1 g in 1 BOTTLE, PLASTIC (0360-0139-01)

• Marketing Start Date: 1997-02-17
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 0360-0139-01 [00360013901]

COCCULUS TABLET

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 1997-02-17

Drug Details

Active Ingredients

Ingredient	Strength
ANAMIRTA COCCULUS SEED	6 [hp_X]/g

OpenFDA Data

• SPL SET ID: 4bf86238-d2a9-4498-e054-00144ff8d46c
• Manufacturer:
  • STANDARD HOMEOPATHIC COMPANY
• UNII:
  • 810258W28U
• UPC Code:
  • 0300360013918

NDC Crossover Matching brand name "COCCULUS" or generic name "Cocculus Ind."

NDC	Brand Name	Generic Name
0360-0139	COCCULUS	COCCULUS IND.
0360-0138	COCCULUS INDICUS	COCCULUS IND.