NDC 43857-0161

Norepinephrine

Norepinephrine

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

• Product ID: 43857-0161_6c128790-08ca-418e-a2c8-e6fda37a620f
• NDC: 43857-0161
• Product Type: Human Otc Drug
• Proprietary Name: Norepinephrine
• Generic Name: Norepinephrine
• Dosage Form: Liquid
• Route of Administration: ORAL
• Marketing Start Date: 2013-04-17
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: BioActive Nutritional, Inc.
• Substance Name: NOREPINEPHRINE
• Active Ingredient Strength: 6 [hp_X]/mL
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 43857-0161-1

30 mL in 1 BOTTLE, DROPPER (43857-0161-1)

• Marketing Start Date: 2013-04-17
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 43857-0161-1 [43857016101]

Norepinephrine LIQUID

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2013-04-17

Drug Details

Active Ingredients

Ingredient	Strength
NOREPINEPHRINE	6 [hp_X]/mL

OpenFDA Data

• SPL SET ID: edf75607-d285-45e5-912e-280d13acbc2b
• Manufacturer:
  • BioActive Nutritional, Inc.
• UNII:
  • X4W3ENH1CV

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

NDC	Brand Name	Generic Name
43742-0101	Norepinephrine	Norepinephrine
43742-0662	Norepinephrine	Norepinephrine
43742-0951	Norepinephrine	Norepinephrine
43742-1319	Norepinephrine	Norepinephrine
43742-1489	Norepinephrine	Norepinephrine (Bitartrate)
43857-0161	Norepinephrine	Norepinephrine
43857-0260	Norepinephrine	Norepinephrine
63083-1530	Norepinephrine	Norepinephrine
44911-0282	Norepinephrine Phenolic	Norepinephrine