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NDC 62135-0702-90 Amoxapine 100 mg/1 Details
Amoxapine 100 mg/1
Amoxapine is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Chartwell RX, LLC. The primary component is AMOXAPINE.
MedlinePlus Drug Summary
Amoxapine is used to treat depression. Amoxapine is in a class of medications called tricyclic antidepressants (TCAs). It works by increasing the amounts of certain natural substances in the brain that are needed to maintain mental balance.
Related Packages: 62135-0702-90Last Updated: 04/28/2024
MedLinePlus Full Drug Details: Amoxapine
Product Information
| NDC | 62135-0702 |
|---|---|
| Product ID | 62135-702_04de67ce-c87b-d4bd-e063-6294a90a4392 |
| Associated GPIs | |
| GCN Sequence Number | 046081 |
| GCN Sequence Number Description | amoxapine TABLET 100 MG ORAL |
| HIC3 | H2U |
| HIC3 Description | TRICYCLIC ANTIDEPRESSANTS,REL.NON-SEL.REUPT-INHIB |
| GCN | 16557 |
| HICL Sequence Number | 001648 |
| HICL Sequence Number Description | AMOXAPINE |
| Brand/Generic | Generic |
| Proprietary Name | Amoxapine |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Amoxapine |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | TABLET |
| Route | ORAL |
| Active Ingredient Strength | 100 |
| Active Ingredient Units | mg/1 |
| Substance Name | AMOXAPINE |
| Labeler Name | Chartwell RX, LLC |
| Pharmaceutical Class | Tricyclic Antidepressant [EPC] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA072878 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 62135-0702-90 (62135070290)
| NDC Package Code | 62135-702-90 |
|---|---|
| Billing NDC | 62135070290 |
| Package | 90 TABLET in 1 BOTTLE (62135-702-90) |
| Marketing Start Date | 2023-09-06 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |