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NDC 70518-1522-00 Nortriptyline Hydrochloride 50 mg/1 Details
Nortriptyline Hydrochloride 50 mg/1
Nortriptyline Hydrochloride is a ORAL CAPSULE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by REMEDYREPACK INC.. The primary component is NORTRIPTYLINE HYDROCHLORIDE.
MedlinePlus Drug Summary
Nortriptyline is used to treat depression. Nortriptyline is in a group of medications called tricyclic antidepressants. It works by increasing the amounts of certain natural substances in the brain that are needed to maintain mental balance.
Related Packages: 70518-1522-00Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Nortriptyline
Product Information
| NDC | 70518-1522 |
|---|---|
| Product ID | 70518-1522_f9dbf3a4-20fe-a847-e053-6394a90ace6d |
| Associated GPIs | |
| GCN Sequence Number | n/a |
| GCN Sequence Number Description | n/a |
| HIC3 | n/a |
| HIC3 Description | n/a |
| GCN | n/a |
| HICL Sequence Number | n/a |
| HICL Sequence Number Description | n/a |
| Brand/Generic | n/a |
| Proprietary Name | Nortriptyline Hydrochloride |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Nortriptyline Hydrochloride |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | CAPSULE |
| Route | ORAL |
| Active Ingredient Strength | 50 |
| Active Ingredient Units | mg/1 |
| Substance Name | NORTRIPTYLINE HYDROCHLORIDE |
| Labeler Name | REMEDYREPACK INC. |
| Pharmaceutical Class | Tricyclic Antidepressant [EPC] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA075520 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 70518-1522-00 (70518152200)
| NDC Package Code | 70518-1522-0 |
|---|---|
| Billing NDC | 70518152200 |
| Package | 30 CAPSULE in 1 BLISTER PACK (70518-1522-0) |
| Marketing Start Date | 2018-10-11 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |