NDC 43742-1489

Norepinephrine

Norepinephrine (bitartrate)

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 Bitartrate.

• Product ID: 43742-1489_0f9decb5-350d-4c6f-a2fe-3385719a3a48
• NDC: 43742-1489
• Product Type: Human Otc Drug
• Proprietary Name: Norepinephrine
• Generic Name: Norepinephrine (bitartrate)
• Dosage Form: Liquid
• Route of Administration: ORAL
• Marketing Start Date: 2019-05-28
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Deseret Biologicals, Inc.
• Substance Name: NOREPINEPHRINE BITARTRATE
• Active Ingredient Strength: 8 [hp_X]/mL
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 43742-1489-1

30 mL in 1 BOTTLE, DROPPER (43742-1489-1)

• Marketing Start Date: 2019-05-28
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 43742-1489-1 [43742148901]

Norepinephrine LIQUID

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2019-05-28

Drug Details

Active Ingredients

Ingredient	Strength
NOREPINEPHRINE BITARTRATE	8 [hp_X]/mL

OpenFDA Data

• SPL SET ID: 8dea9818-e3f1-4c51-9e67-83a63f3e950c
• Manufacturer:
  • Deseret Biologicals, Inc.
• UNII:
  • IFY5PE3ZRW

NDC Crossover Matching brand name "Norepinephrine" or generic name "Norepinephrine (bitartrate)"

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
44911-0499	Norepinephrine Phenolic	Norepinephrine (Bitartrate)