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NDC 00781-8974-01 Desipramine Hydrochloride 75 mg/1 Details
Desipramine Hydrochloride 75 mg/1
Desipramine Hydrochloride is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Sandoz Inc. The primary component is DESIPRAMINE HYDROCHLORIDE.
MedlinePlus Drug Summary
Desipramine is used to treat depression. Desipramine is in a class of medications called tricyclic antidepressants. It works by increasing the amounts of certain natural substances in the brain that are needed for mental balance.
Related Packages: 00781-8974-01Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Desipramine
Product Information
NDC | 00781-8974 |
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Product ID | 0781-8974_b04d3bbb-6154-41f7-bc95-318ae2e9a800 |
Associated GPIs | 58200030100320 |
GCN Sequence Number | 046108 |
GCN Sequence Number Description | desipramine HCl TABLET 75 MG ORAL |
HIC3 | H2U |
HIC3 Description | TRICYCLIC ANTIDEPRESSANTS,REL.NON-SEL.REUPT-INHIB |
GCN | 16588 |
HICL Sequence Number | 001645 |
HICL Sequence Number Description | DESIPRAMINE HCL |
Brand/Generic | Generic |
Proprietary Name | Desipramine Hydrochloride |
Proprietary Name Suffix | n/a |
Non-Proprietary Name | Desipramine Hydrochloride |
Product Type | HUMAN PRESCRIPTION DRUG |
Dosage Form | TABLET, FILM COATED |
Route | ORAL |
Active Ingredient Strength | 75 |
Active Ingredient Units | mg/1 |
Substance Name | DESIPRAMINE HYDROCHLORIDE |
Labeler Name | Sandoz Inc |
Pharmaceutical Class | Tricyclic Antidepressant [EPC] |
DEA Schedule | n/a |
Marketing Category | ANDA |
Application Number | ANDA072102 |
Listing Certified Through | n/a |
Package
NDC 00781-8974-01 (00781897401)
NDC Package Code | 0781-8974-01 |
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Billing NDC | 00781897401 |
Package | 100 TABLET, FILM COATED in 1 BOTTLE (0781-8974-01) |
Marketing Start Date | 2018-06-27 |
NDC Exclude Flag | N |
Pricing Information | N/A |