Product NDC: | 42799-217 |
Proprietary Name: | Opium Tincture Deodorized |
Non Proprietary Name: | Morphine |
Active Ingredient(s): | 10 mg/mL & nbsp; Morphine |
Administration Route(s): | ORAL |
Dosage Form(s): | TINCTURE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 42799-217 |
Labeler Name: | Edenbridge Pharmaceuticals, LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 20100715 |
Package NDC: | 42799-217-02 |
Package Description: | 473 mL in 1 BOTTLE, PLASTIC (42799-217-02) |
NDC Code | 42799-217-02 |
Proprietary Name | Opium Tincture Deodorized |
Package Description | 473 mL in 1 BOTTLE, PLASTIC (42799-217-02) |
Product NDC | 42799-217 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Morphine |
Dosage Form Name | TINCTURE |
Route Name | ORAL |
Start Marketing Date | 20100715 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | Edenbridge Pharmaceuticals, LLC |
Substance Name | MORPHINE |
Strength Number | 10 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |