| Product NDC: | 0574-0159 |
| 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: | 0574-0159 |
| Labeler Name: | Paddock Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20110128 |
| Package NDC: | 0574-0159-04 |
| Package Description: | 118 mL in 1 BOTTLE (0574-0159-04) |
| NDC Code | 0574-0159-04 |
| Proprietary Name | OPIUM TINCTURE DEODORIZED |
| Package Description | 118 mL in 1 BOTTLE (0574-0159-04) |
| Product NDC | 0574-0159 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Morphine |
| Dosage Form Name | TINCTURE |
| Route Name | ORAL |
| Start Marketing Date | 20110128 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Paddock Laboratories, Inc. |
| Substance Name | MORPHINE |
| Strength Number | 10 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |