NDC 10191-1089

OPIUM

Raw Opium Gum

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

• Product ID: 10191-1089_1a7658ae-18ff-0bca-e054-00144ff88e88
• NDC: 10191-1089
• Product Type: Human Prescription Drug
• Proprietary Name: OPIUM
• Generic Name: Raw Opium Gum
• Dosage Form: Pellet
• Route of Administration: SUBLINGUAL
• Marketing Start Date: 2015-07-09
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Remedy Makers
• Substance Name: OPIUM
• Active Ingredient Strength: 6 [hp_C]/1
• DEA Schedule: CII
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 10191-1089-2

166 PELLET in 1 VIAL, GLASS (10191-1089-2)

• Marketing Start Date: 2015-07-09
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 10191-1089-2 [10191108902]

OPIUM PELLET

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2015-07-09
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
OPIUM	6 [hp_C]/1

OpenFDA Data

• SPL SET ID: 1a7658ae-18fe-0bca-e054-00144ff88e88
• Manufacturer:
  • Remedy Makers
• UNII:
  • 37M3MZ001L
• UPC Code:
  • 0310191108929

NDC Crossover Matching brand name "OPIUM" or generic name "Raw Opium Gum"

NDC	Brand Name	Generic Name
10191-1081	OPIUM	Raw Opium Gum
10191-1082	OPIUM	Raw Opium Gum
10191-1086	OPIUM	Raw Opium Gum
10191-1089	OPIUM	Raw Opium Gum
10191-1093	OPIUM	RAW OPIUM GUM
69152-1111	Opium 30C	Opium