Opium Tincture Deodorized is a Oral Solution in the Human Prescription Drug category. It is labeled and distributed by Valeant Pharmaceuticals North America Llc. The primary component is Morphine.
Product ID | 0187-4203_3ad95865-a77c-41da-b572-e5c0bb404c79 |
NDC | 0187-4203 |
Product Type | Human Prescription Drug |
Proprietary Name | Opium Tincture Deodorized |
Generic Name | Morphine |
Dosage Form | Solution |
Route of Administration | ORAL |
Marketing Start Date | 2008-09-17 |
Marketing Category | UNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER |
Labeler Name | Valeant Pharmaceuticals North America LLC |
Substance Name | MORPHINE |
Active Ingredient Strength | 10 mg/mL |
Pharm Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
DEA Schedule | CII |
NDC Exclude Flag | N |
Listing Certified Through | 2019-12-31 |
Marketing Start Date | 2008-09-17 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | Unapproved drug other |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | ML |
Marketing Start Date | 2008-09-17 |
Inactivation Date | 2020-01-31 |
Marketing Category | Unapproved drug other |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | ML |
Marketing Start Date | 2008-09-17 |
Inactivation Date | 2020-01-31 |
Ingredient | Strength |
---|---|
MORPHINE | 10 mg/mL |
SPL SET ID: | 3ad95865-a77c-41da-b572-e5c0bb404c79 |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI |
NDC | Brand Name | Generic Name |
---|---|---|
0187-4203 | Opium Tincture Deodorized | morphine |
42799-217 | Opium Tincture Deodorized | Morphine |
62559-153 | Opium Tincture Deodorized | morphine tincture |
63629-1965 | Opium Tincture Deodorized | morphine tincture |
10191-1001 | MORPHINUM | MORPHINE |
10191-1002 | MORPHINUM | MORPHINE |
10191-1003 | MORPHINUM | MORPHINE |
10191-1004 | MORPHINUM | MORPHINE |
10191-1005 | MORPHINUM | MORPHINE |