NDC 43742-1319

Norepinephrine

Norepinephrine

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

• Product ID: 43742-1319_6eae03af-c907-4651-85b2-7a6bcb2c9974
• NDC: 43742-1319
• Product Type: Human Otc Drug
• Proprietary Name: Norepinephrine
• Generic Name: Norepinephrine
• Dosage Form: Liquid
• Route of Administration: ORAL
• Marketing Start Date: 2018-09-19
• Marketing End Date: 2024-02-04
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Deseret Biologicals, Inc.
• Substance Name: NOREPINEPHRINE
• Active Ingredient Strength: 8 [hp_X]/mL
• Pharm Classes: Catecholamine [EPC], Catecholamines [CS]
• NDC Exclude Flag: N

Packaging

NDC 43742-1319-1

30 mL in 1 BOTTLE, DROPPER (43742-1319-1)

• Marketing Start Date: 2018-09-19
• Marketing End Date: 2024-02-04
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 43742-1319-1 [43742131901]

Norepinephrine LIQUID

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2018-09-19

Drug Details

Active Ingredients

Ingredient	Strength
NOREPINEPHRINE	8 [hp_X]/mL

OpenFDA Data

• SPL SET ID: 154d38ee-e3e8-48eb-8ad9-0ae966ab39e5
• Manufacturer:
  • Deseret Biologicals, 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