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Protriptyline Hydrochloride
Protriptyline Hydrochloride - 64980-159-01 - (Protriptyline Hydrochloride)
Drug Information of Protriptyline Hydrochloride
| Product NDC: | 64980-159 |
| Proprietary Name: | Protriptyline Hydrochloride |
| Non Proprietary Name: | Protriptyline Hydrochloride |
| Active Ingredient(s): | 10 mg/1 & nbsp; Protriptyline Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Protriptyline Hydrochloride
| Product NDC: | 64980-159 |
| Labeler Name: | Rising Pharmaceuticals, Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA090462 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100611 |
Package Information of Protriptyline Hydrochloride
| Package NDC: | 64980-159-01 |
| Package Description: | 100 TABLET, FILM COATED in 1 BOTTLE (64980-159-01) |
NDC Information of Protriptyline Hydrochloride
| NDC Code | 64980-159-01 |
| Proprietary Name | Protriptyline Hydrochloride |
| Package Description | 100 TABLET, FILM COATED in 1 BOTTLE (64980-159-01) |
| Product NDC | 64980-159 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Protriptyline Hydrochloride |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20100611 |
| Marketing Category Name | ANDA |
| Labeler Name | Rising Pharmaceuticals, Inc |
| Substance Name | PROTRIPTYLINE HYDROCHLORIDE |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Tricyclic Antidepressant [EPC] |
