NDC 60512-6158

ADRENOCORTICOTROPHIN

Adrenocorticotrophin

ADRENOCORTICOTROPHIN is a Oral Pellet in the Human Otc Drug category. It is labeled and distributed by Homeolab Usa Inc.. The primary component is Corticotropin.

• Product ID: 60512-6158_f0c6c22e-405e-4840-8696-e28246cee59d
• NDC: 60512-6158
• Product Type: Human Otc Drug
• Proprietary Name: ADRENOCORTICOTROPHIN
• Generic Name: Adrenocorticotrophin
• 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: CORTICOTROPIN
• Active Ingredient Strength: 6 [hp_X]/1
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 60512-6158-1

80 PELLET in 1 TUBE (60512-6158-1)

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

NDC SPL Data Element Entries

NDC 60512-6158-1 [60512615801]

ADRENOCORTICOTROPHIN 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
CORTICOTROPIN	6 [hp_X]/1

OpenFDA Data

• SPL SET ID: 7cc94bcb-115c-4e27-b463-e1ecee300513
• Manufacturer:
  • HOMEOLAB USA INC.
• UNII:
  • K0U68Q2TXA

NDC Crossover Matching brand name "ADRENOCORTICOTROPHIN" or generic name "Adrenocorticotrophin"

NDC	Brand Name	Generic Name
60512-6158	ADRENOCORTICOTROPHIN	ADRENOCORTICOTROPHIN
68428-181	Adrenocorticotrophin	CORTICOTROPIN
71919-015	Adrenocorticotrophin	CORTICOTROPIN