desipramine hydrochloride

Generic: desipramine hydrochloride

Labeler: ingenus pharmaceuticals, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name desipramine hydrochloride
Generic Name desipramine hydrochloride
Labeler ingenus pharmaceuticals, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

desipramine hydrochloride 10 mg/1

Manufacturer
Ingenus Pharmaceuticals, LLC

Identifiers & Regulatory

Product NDC 50742-112
Product ID 50742-112_7a0e5dd9-7456-4774-b529-ce9d5627b654
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA204963
Listing Expiration 2026-12-31
Marketing Start 2018-09-19

Pharmacologic Class

Classes
tricyclic antidepressant [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 50742112
Hyphenated Format 50742-112

Supplemental Identifiers

RxCUI
1099288 1099292 1099296 1099300 1099304 1099316
UPC
0350742112012 0350742116010 0350742114016 0350742117505 0350742113019 0350742115013
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 hydrochloride (source: ndc)
Application Number ANDA204963 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (50742-112-01)
source: ndc

Packages (1)

50742-112-01 100 TABLET in 1 BOTTLE (50742-112-01)

Ingredients (1)

desipramine hydrochloride (10 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": "7a0e5dd9-7456-4774-b529-ce9d5627b654", "openfda": {"upc": ["0350742112012", "0350742116010", "0350742114016", "0350742117505", "0350742113019", "0350742115013"], "unii": ["1Y58DO4MY1"], "rxcui": ["1099288", "1099292", "1099296", "1099300", "1099304", "1099316"], "spl_set_id": ["7280f157-3fff-41c5-b3f4-510b8bacdaba"], "manufacturer_name": ["Ingenus Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (50742-112-01)", "package_ndc": "50742-112-01", "marketing_start_date": "20180919"}], "brand_name": "DESIPRAMINE HYDROCHLORIDE", "product_id": "50742-112_7a0e5dd9-7456-4774-b529-ce9d5627b654", "dosage_form": "TABLET", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "50742-112", "generic_name": "desipramine hydrochloride", "labeler_name": "Ingenus Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DESIPRAMINE HYDROCHLORIDE", "active_ingredients": [{"name": "DESIPRAMINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA204963", "marketing_category": "ANDA", "marketing_start_date": "20180919", "listing_expiration_date": "20261231"}