NDC 44911-0282

Norepinephrine Phenolic

Norepinephrine

Norepinephrine Phenolic is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Energique, Inc.. The primary component is Norepinephrine.

• Product ID: 44911-0282_229f4395-f9de-4fa7-9845-5b13a9368772
• NDC: 44911-0282
• Product Type: Human Otc Drug
• Proprietary Name: Norepinephrine Phenolic
• Generic Name: Norepinephrine
• Dosage Form: Liquid
• Route of Administration: ORAL
• Marketing Start Date: 2015-10-26
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Energique, Inc.
• Substance Name: NOREPINEPHRINE
• Active Ingredient Strength: 6 [hp_X]/mL
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 44911-0282-1

30 mL in 1 BOTTLE, DROPPER (44911-0282-1)

• Marketing Start Date: 2015-10-26
• Marketing End Date: 2022-05-16
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 44911-0282-1 [44911028201]

Norepinephrine Phenolic LIQUID

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2015-10-26
• Marketing End Date: 2022-05-16
• Inactivation Date: 2020-01-31
• Reactivation Date: 2020-04-09

Drug Details

Active Ingredients

Ingredient	Strength
NOREPINEPHRINE	6 [hp_X]/mL

OpenFDA Data

• SPL SET ID: e82e3fb5-65f8-415f-bc98-3f9cf3111164
• Manufacturer:
  • Energique, Inc.
• UNII:
  • X4W3ENH1CV

NDC Crossover Matching brand name "Norepinephrine Phenolic" or generic name "Norepinephrine"

NDC	Brand Name	Generic Name
44911-0282	Norepinephrine Phenolic	Norepinephrine
44911-0499	Norepinephrine Phenolic	Norepinephrine (Bitartrate)
43742-0101	Norepinephrine	Norepinephrine
43742-0662	Norepinephrine	Norepinephrine
43742-0951	Norepinephrine	Norepinephrine
43742-1319	Norepinephrine	Norepinephrine
43857-0161	Norepinephrine	Norepinephrine
43857-0260	Norepinephrine	Norepinephrine
63083-1530	Norepinephrine	Norepinephrine