NDC 10191-1013

MORPHINUM

Morphine Base

MORPHINUM is a Sublingual Pellet in the Human Prescription Drug category. It is labeled and distributed by Remedy Makers. The primary component is Morphine.

• Product ID: 10191-1013_cab6232e-4cd9-4c73-989e-13a5246869c5
• NDC: 10191-1013
• Product Type: Human Prescription Drug
• Proprietary Name: MORPHINUM
• Generic Name: Morphine Base
• Dosage Form: Pellet
• Route of Administration: SUBLINGUAL
• Marketing Start Date: 2001-04-27
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Remedy Makers
• Substance Name: MORPHINE
• Active Ingredient Strength: 30 [hp_C]/1
• Pharm Classes: Full Opioid Agonists [MoA],Opioid Agonist [EPC]
• DEA Schedule: CII
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 10191-1013-2

151 PELLET in 1 VIAL, GLASS (10191-1013-2)

• Marketing Start Date: 2001-04-27
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 10191-1013-2 [10191101302]

MORPHINUM PELLET

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2001-04-27
• Inactivation Date: 2019-10-29

Drug Details

Active Ingredients

Ingredient	Strength
MORPHINE	30 [hp_C]/1

OpenFDA Data

• SPL SET ID: b02b0b9b-e73a-4c50-8e80-38688841b935
• Manufacturer:
  • Remedy Makers
• UNII:
  • 76I7G6D29C
• UPC Code:
  • 0310191101326

Pharmacological Class

• Full Opioid Agonists [MoA]
• Opioid Agonist [EPC]

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

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