NDC 60512-6157

ADRENALINUM

Adrenalinum

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

• Product ID: 60512-6157_0787ef5a-1f3d-405f-8048-4d1bf1a821b4
• NDC: 60512-6157
• Product Type: Human Otc Drug
• Proprietary Name: ADRENALINUM
• Generic Name: Adrenalinum
• 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: EPINEPHRINE
• Active Ingredient Strength: 6 [hp_X]/1
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 60512-6157-1

80 PELLET in 1 TUBE (60512-6157-1)

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

NDC SPL Data Element Entries

NDC 60512-6157-1 [60512615701]

ADRENALINUM 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
EPINEPHRINE	6 [hp_X]/1

OpenFDA Data

• SPL SET ID: 6ed9f6fc-be53-4bb1-9edf-61a2be1ff02d
• Manufacturer:
  • HOMEOLAB USA INC.
• UNII:
  • YKH834O4BH

NDC Crossover Matching brand name "ADRENALINUM" or generic name "Adrenalinum"

NDC	Brand Name	Generic Name
0220-0076	Adrenalinum	EPINEPHRINE
0220-0078	Adrenalinum	EPINEPHRINE
15631-0007	ADRENALINUM	ADRENALINUM
60512-6157	ADRENALINUM	ADRENALINUM
66096-778	Adrenalinum	ADRENALINUM
68428-180	Adrenalinum	EPINEPHRINE
71919-014	Adrenalinum	EPINEPHRINE
43742-0728	Epinephrine	Adrenalinum
43742-1243	Epinephrine	Adrenalinum