| Product NDC: | 64038-059 |
| Proprietary Name: | Tramapap |
| Non Proprietary Name: | Tramadol Hydrochloride, Acetaminophen |
| Active Ingredient(s): | & nbsp; Tramadol Hydrochloride, Acetaminophen |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 64038-059 |
| Labeler Name: | Living Well Pharmacy, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20100407 |
| Package NDC: | 64038-059-03 |
| Package Description: | 1 KIT in 1 KIT (64038-059-03) * 15 g in 1 BOTTLE (64038-738-15) * 75 g in 1 BOTTLE (64038-135-75) |
| NDC Code | 64038-059-03 |
| Proprietary Name | Tramapap |
| Package Description | 1 KIT in 1 KIT (64038-059-03) * 15 g in 1 BOTTLE (64038-738-15) * 75 g in 1 BOTTLE (64038-135-75) |
| Product NDC | 64038-059 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Tramadol Hydrochloride, Acetaminophen |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20100407 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Living Well Pharmacy, Inc. |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
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