NDC 43742-0839

Pyrrole

Pyrrole

Pyrrole is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Deseret Biologicals, Inc.. The primary component is Pyrrole.

• Product ID: 43742-0839_c09af948-f921-4ca9-b5de-77db39b1452d
• NDC: 43742-0839
• Product Type: Human Otc Drug
• Proprietary Name: Pyrrole
• Generic Name: Pyrrole
• Dosage Form: Liquid
• Route of Administration: ORAL
• Marketing Start Date: 2016-09-07
• Marketing End Date: 2023-06-25
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Deseret Biologicals, Inc.
• Substance Name: PYRROLE
• Active Ingredient Strength: 6 [hp_X]/mL
• NDC Exclude Flag: N

Packaging

NDC 43742-0839-1

30 mL in 1 BOTTLE, DROPPER (43742-0839-1)

• Marketing Start Date: 2016-09-07
• Marketing End Date: 2023-06-25
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 43742-0839-1 [43742083901]

Pyrrole LIQUID

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2016-09-07
• Marketing End Date: 2023-06-25

Drug Details

Active Ingredients

Ingredient	Strength
PYRROLE	6 [hp_X]/mL

OpenFDA Data

• SPL SET ID: 0061b8a6-a8c8-4047-8f68-6f8002b19ff0
• Manufacturer:
  • Deseret Biologicals, Inc.
• UNII:
  • 86S1ZD6L2C

NDC Crossover Matching brand name "Pyrrole" or generic name "Pyrrole"

NDC	Brand Name	Generic Name
43742-0221	Pyrrole	Pyrrole
43742-0839	Pyrrole	Pyrrole
43742-1323	Pyrrole	Pyrrole
63083-1539	Pyrrole	Pyrrole