NDC 43742-1323

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: 43742-1323_37f827d9-5b14-4114-8f32-f8ca635ef749
• NDC: 43742-1323
• Product Type: Human Otc Drug
• Proprietary Name: Pyrrole
• Generic Name: Pyrrole
• Dosage Form: Liquid
• Route of Administration: ORAL
• Marketing Start Date: 2020-03-18
• Marketing End Date: 2025-03-26
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Deseret Biologicals, Inc.
• Substance Name: PYRROLE
• Active Ingredient Strength: 8 [hp_X]/mL
• NDC Exclude Flag: N

Packaging

NDC 43742-1323-1

30 mL in 1 BOTTLE, DROPPER (43742-1323-1)

• Marketing Start Date: 2020-03-18
• Marketing End Date: 2025-03-26
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 43742-1323-1 [43742132301]

Pyrrole LIQUID

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2020-03-18

Drug Details

Active Ingredients

Ingredient	Strength
PYRROLE	8 [hp_X]/mL

OpenFDA Data

• SPL SET ID: 81fbcf59-44b0-4639-ae20-6b94697b5b6c
• 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