desipramine hydrochloride

Generic: desipramine

Labeler: amneal pharmaceuticals ny llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name desipramine hydrochloride
Generic Name desipramine
Labeler amneal pharmaceuticals ny llc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

desipramine hydrochloride 75 mg/1

Manufacturer
Amneal Pharmaceuticals NY LLC

Identifiers & Regulatory

Product NDC 69238-1059
Product ID 69238-1059_34a146f8-ed42-4e1c-9c22-6c81f6ef09f9
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA208105
Listing Expiration 2026-12-31
Marketing Start 2016-03-21

Pharmacologic Class

Classes
tricyclic antidepressant [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 692381059
Hyphenated Format 69238-1059

Supplemental Identifiers

RxCUI
1099288 1099292 1099296 1099300 1099304 1099316
UNII
1Y58DO4MY1

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name desipramine hydrochloride (source: ndc)
Generic Name desipramine (source: ndc)
Application Number ANDA208105 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 75 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE (69238-1059-1)
  • 30 TABLET, FILM COATED in 1 BOTTLE (69238-1059-3)
source: ndc

Packages (2)

69238-1059-1 100 TABLET, FILM COATED in 1 BOTTLE (69238-1059-1) 69238-1059-3 30 TABLET, FILM COATED in 1 BOTTLE (69238-1059-3)

Ingredients (1)

desipramine hydrochloride (75 mg/1)

Linked Drug Pages (1)

Desipramine Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "34a146f8-ed42-4e1c-9c22-6c81f6ef09f9", "openfda": {"unii": ["1Y58DO4MY1"], "rxcui": ["1099288", "1099292", "1099296", "1099300", "1099304", "1099316"], "spl_set_id": ["a3b4b25d-0ddb-4531-badb-f1ba3168ac07"], "manufacturer_name": ["Amneal Pharmaceuticals NY LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (69238-1059-1)", "package_ndc": "69238-1059-1", "marketing_start_date": "20160321"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (69238-1059-3)", "package_ndc": "69238-1059-3", "marketing_start_date": "20160321"}], "brand_name": "Desipramine Hydrochloride", "product_id": "69238-1059_34a146f8-ed42-4e1c-9c22-6c81f6ef09f9", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "69238-1059", "generic_name": "Desipramine", "labeler_name": "Amneal Pharmaceuticals NY LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Desipramine Hydrochloride", "active_ingredients": [{"name": "DESIPRAMINE HYDROCHLORIDE", "strength": "75 mg/1"}], "application_number": "ANDA208105", "marketing_category": "ANDA", "marketing_start_date": "20160321", "listing_expiration_date": "20261231"}