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Nortriptyline Hydrochloride
Nortriptyline Hydrochloride - 0121-0678-16 - (Nortriptyline Hydrochloride)
Drug Information of Nortriptyline Hydrochloride
| Product NDC: | 0121-0678 |
| Proprietary Name: | Nortriptyline Hydrochloride |
| Non Proprietary Name: | Nortriptyline Hydrochloride |
| Active Ingredient(s): | 10 mg/5mL & nbsp; Nortriptyline Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Nortriptyline Hydrochloride
| Product NDC: | 0121-0678 |
| Labeler Name: | Pharmaceutical Associates, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075606 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20000823 |
Package Information of Nortriptyline Hydrochloride
| Package NDC: | 0121-0678-16 |
| Package Description: | 473 mL in 1 BOTTLE (0121-0678-16) |
NDC Information of Nortriptyline Hydrochloride
| NDC Code | 0121-0678-16 |
| Proprietary Name | Nortriptyline Hydrochloride |
| Package Description | 473 mL in 1 BOTTLE (0121-0678-16) |
| Product NDC | 0121-0678 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Nortriptyline Hydrochloride |
| Dosage Form Name | SOLUTION |
| Route Name | ORAL |
| Start Marketing Date | 20000823 |
| Marketing Category Name | ANDA |
| Labeler Name | Pharmaceutical Associates, Inc. |
| Substance Name | NORTRIPTYLINE HYDROCHLORIDE |
| Strength Number | 10 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes | Tricyclic Antidepressant [EPC] |
