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Protriptyline Hydrochloride
Protriptyline Hydrochloride - 0555-0595-02 - (Protriptyline Hydrochloride)
Drug Information of Protriptyline Hydrochloride
| Product NDC: | 0555-0595 |
| Proprietary Name: | Protriptyline Hydrochloride |
| Non Proprietary Name: | Protriptyline Hydrochloride |
| Active Ingredient(s): | 5 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: | 0555-0595 |
| Labeler Name: | Barr Laboratories Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA073644 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20081223 |
Package Information of Protriptyline Hydrochloride
| Package NDC: | 0555-0595-02 |
| Package Description: | 100 TABLET, FILM COATED in 1 BOTTLE (0555-0595-02) |
NDC Information of Protriptyline Hydrochloride
| NDC Code | 0555-0595-02 |
| Proprietary Name | Protriptyline Hydrochloride |
| Package Description | 100 TABLET, FILM COATED in 1 BOTTLE (0555-0595-02) |
| Product NDC | 0555-0595 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Protriptyline Hydrochloride |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20081223 |
| Marketing Category Name | ANDA |
| Labeler Name | Barr Laboratories Inc. |
| Substance Name | PROTRIPTYLINE HYDROCHLORIDE |
| Strength Number | 5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Tricyclic Antidepressant [EPC] |
