| 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] |