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NDC 42806-0097-01 Protriptyline Hydrochloride 10 mg/1 Details
Protriptyline Hydrochloride 10 mg/1
Protriptyline Hydrochloride is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Epic Pharma, LLC. The primary component is PROTRIPTYLINE HYDROCHLORIDE.
MedlinePlus Drug Summary
Protriptyline is used to treat depression. Protriptyline is in a class of medications called tricyclic antidepressants. It works by increasing the amounts of certain natural substances in the brain that help maintain mental balance.
Related Packages: 42806-0097-01Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Protriptyline
Product Information
| NDC | 42806-0097 |
|---|---|
| Product ID | 42806-097_e68d74c7-1d6a-4453-bb46-0047047b7527 |
| Associated GPIs | 58200070100310 |
| GCN Sequence Number | 046079 |
| GCN Sequence Number Description | protriptyline HCl TABLET 10 MG ORAL |
| HIC3 | H2U |
| HIC3 Description | TRICYCLIC ANTIDEPRESSANTS,REL.NON-SEL.REUPT-INHIB |
| GCN | 16555 |
| HICL Sequence Number | 001646 |
| HICL Sequence Number Description | PROTRIPTYLINE HCL |
| Brand/Generic | Generic |
| Proprietary Name | Protriptyline Hydrochloride |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Protriptyline Hydrochloride |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | TABLET, FILM COATED |
| Route | ORAL |
| Active Ingredient Strength | 10 |
| Active Ingredient Units | mg/1 |
| Substance Name | PROTRIPTYLINE HYDROCHLORIDE |
| Labeler Name | Epic Pharma, LLC |
| Pharmaceutical Class | Tricyclic Antidepressant [EPC] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA202220 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 42806-0097-01 (42806009701)
| NDC Package Code | 42806-097-01 |
|---|---|
| Billing NDC | 42806009701 |
| Package | 100 TABLET, FILM COATED in 1 BOTTLE (42806-097-01) |
| Marketing Start Date | 2013-01-09 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |