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Opium Tincture (Deodorized)
Opium Tincture (Deodorized) - 42998-203-01 - (Morphine (anhydrous))
Drug Information of Opium Tincture (Deodorized)
| Product NDC: | 42998-203 |
| Proprietary Name: | Opium Tincture (Deodorized) |
| Non Proprietary Name: | Morphine (anhydrous) |
| Active Ingredient(s): | 10 mg/mL & nbsp; Morphine (anhydrous) |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Opium Tincture (Deodorized)
| Product NDC: | 42998-203 |
| Labeler Name: | Marathon Pharmaceuticals, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20080925 |
Package Information of Opium Tincture (Deodorized)
| Package NDC: | 42998-203-01 |
| Package Description: | 118 mL in 1 BOTTLE, GLASS (42998-203-01) |
NDC Information of Opium Tincture (Deodorized)
| NDC Code | 42998-203-01 |
| Proprietary Name | Opium Tincture (Deodorized) |
| Package Description | 118 mL in 1 BOTTLE, GLASS (42998-203-01) |
| Product NDC | 42998-203 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Morphine (anhydrous) |
| Dosage Form Name | SOLUTION |
| Route Name | ORAL |
| Start Marketing Date | 20080925 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Marathon Pharmaceuticals, LLC |
| Substance Name | MORPHINE |
| Strength Number | 10 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
