NDC 10191-1029

Morphinum Muriaticum

Morphine Hydrochloride

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

• Product ID: 10191-1029_26d4e1a1-94cf-44b8-b83a-8be26c36376e
• NDC: 10191-1029
• Product Type: Human Prescription Drug
• Proprietary Name: Morphinum Muriaticum
• Generic Name: Morphine Hydrochloride
• Dosage Form: Pellet
• Route of Administration: SUBLINGUAL
• Marketing Start Date: 2002-04-09
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Remedy Makers
• Substance Name: MORPHINE HYDROCHLORIDE
• 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 10191-1029-2

130 PELLET in 1 VIAL, GLASS (10191-1029-2)

• Marketing Start Date: 2002-04-09
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 10191-1029-2 [10191102902]

Morphinum Muriaticum PELLET

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2002-04-09
• Inactivation Date: 2019-10-29

Drug Details

Active Ingredients

Ingredient	Strength
MORPHINE HYDROCHLORIDE	30 [hp_C]/1

OpenFDA Data

• SPL SET ID: fdfbfc04-5473-404d-b1c8-a035beb1fe6c
• Manufacturer:
  • Remedy Makers
• UNII:
  • J28GE0ROVX
• UPC Code:
  • 0310191102927

Pharmacological Class

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