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Nortriptyline Hydrochloride
Nortriptyline Hydrochloride - 51672-4004-5 - (Nortriptyline Hydrochloride)
Drug Information of Nortriptyline Hydrochloride
| Product NDC: | 51672-4004 |
| Proprietary Name: | Nortriptyline Hydrochloride |
| Non Proprietary Name: | Nortriptyline Hydrochloride |
| Active Ingredient(s): | 75 mg/1 & nbsp; Nortriptyline Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Nortriptyline Hydrochloride
| Product NDC: | 51672-4004 |
| Labeler Name: | Taro Pharmaceuticals U.S.A., Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075520 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20000508 |
Package Information of Nortriptyline Hydrochloride
| Package NDC: | 51672-4004-5 |
| Package Description: | 90 CAPSULE in 1 BOTTLE (51672-4004-5) |
NDC Information of Nortriptyline Hydrochloride
| NDC Code | 51672-4004-5 |
| Proprietary Name | Nortriptyline Hydrochloride |
| Package Description | 90 CAPSULE in 1 BOTTLE (51672-4004-5) |
| Product NDC | 51672-4004 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Nortriptyline Hydrochloride |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20000508 |
| Marketing Category Name | ANDA |
| Labeler Name | Taro Pharmaceuticals U.S.A., Inc. |
| Substance Name | NORTRIPTYLINE HYDROCHLORIDE |
| Strength Number | 75 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Tricyclic Antidepressant [EPC] |
