NDC 66096-778

Adrenalinum

Adrenalinum

Adrenalinum is a Oral Pellet in the Human Otc Drug category. It is labeled and distributed by Ohm Pharma Inc.. The primary component is Epinephrine.

• Product ID: 66096-778_b3755fd7-de94-4c39-8f84-94ccd4771606
• NDC: 66096-778
• Product Type: Human Otc Drug
• Proprietary Name: Adrenalinum
• Generic Name: Adrenalinum
• Dosage Form: Pellet
• Route of Administration: ORAL
• Marketing Start Date: 2019-11-01
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: OHM PHARMA INC.
• Substance Name: EPINEPHRINE
• Active Ingredient Strength: 6 [hp_C]/6[hp_C]
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 66096-778-01

6 [hp_C] in 1 TUBE (66096-778-01)

• Marketing Start Date: 2019-11-01
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 66096-778-01 [66096077801]

Adrenalinum PELLET

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2019-11-01

Drug Details

Active Ingredients

Ingredient	Strength
EPINEPHRINE	6 [hp_C]/6[hp_C]

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