NDC 10191-1001

MORPHINUM

Morphine

MORPHINUM is a Sublingual Pellet in the Human Prescription Drug category. It is labeled and distributed by Remedy Makers. The primary component is Abt-925 Anhydrous Free Base.

• Product ID: 10191-1001_1c6d882b-4f2d-2cfb-e054-00144ff88e88
• NDC: 10191-1001
• Product Type: Human Prescription Drug
• Proprietary Name: MORPHINUM
• Generic Name: Morphine
• Dosage Form: Pellet
• Route of Administration: SUBLINGUAL
• Marketing Start Date: 2015-07-22
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Remedy Makers
• Substance Name: ABT-925 ANHYDROUS FREE BASE
• Active Ingredient Strength: 3 [hp_X]/1
• DEA Schedule: CII
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 10191-1001-2

162 PELLET in 1 VIAL, GLASS (10191-1001-2)

• Marketing Start Date: 2015-07-22
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 10191-1001-2 [10191100102]

MORPHINUM PELLET

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2015-07-22
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
ABT-925 ANHYDROUS FREE BASE	3 [hp_X]/1

OpenFDA Data

• SPL SET ID: 1c6d882b-4f2c-2cfb-e054-00144ff88e88
• Manufacturer:
  • Remedy Makers
• UNII:
  • E6CKI5C54O
• UPC Code:
  • 0310191100121

NDC Crossover Matching brand name "MORPHINUM" or generic name "Morphine"

NDC	Brand Name	Generic Name
10191-1001	MORPHINUM	MORPHINE
10191-1002	MORPHINUM	MORPHINE
10191-1003	MORPHINUM	MORPHINE
10191-1004	MORPHINUM	MORPHINE
10191-1005	MORPHINUM	MORPHINE
10191-1013	MORPHINUM	MORPHINE BASE
0187-4203	Opium Tincture Deodorized	morphine
42799-217	Opium Tincture Deodorized	Morphine