| Product NDC: | 0406-9910 |
| Proprietary Name: | PAMELOR |
| Non Proprietary Name: | nortriptyline hydrochloride |
| Active Ingredient(s): | 10 mg/1 & nbsp; nortriptyline hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 0406-9910 |
| Labeler Name: | Mallinckrodt, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA018013 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20100803 |
| Package NDC: | 0406-9910-03 |
| Package Description: | 30 CAPSULE in 1 BOTTLE (0406-9910-03) |
| NDC Code | 0406-9910-03 |
| Proprietary Name | PAMELOR |
| Package Description | 30 CAPSULE in 1 BOTTLE (0406-9910-03) |
| Product NDC | 0406-9910 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | nortriptyline hydrochloride |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20100803 |
| Marketing Category Name | NDA |
| Labeler Name | Mallinckrodt, Inc. |
| Substance Name | NORTRIPTYLINE HYDROCHLORIDE |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Tricyclic Antidepressant [EPC] |