desipramine hydrochloride

Generic: desipramine hydrochloride

Labeler: alembic pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name desipramine hydrochloride
Generic Name desipramine hydrochloride
Labeler alembic pharmaceuticals inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

desipramine hydrochloride 100 mg/1

Manufacturer
Alembic Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 62332-319
Product ID 62332-319_06c52509-29c8-41c5-8492-3458df75f3d5
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA209785
Listing Expiration 2026-12-31
Marketing Start 2021-07-08

Pharmacologic Class

Classes
tricyclic antidepressant [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 62332319
Hyphenated Format 62332-319

Supplemental Identifiers

RxCUI
1099288 1099292 1099296 1099300 1099304 1099316
UPC
0362332320318
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 ANDA209785 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (62332-319-30)
  • 100 TABLET, FILM COATED in 1 BOTTLE (62332-319-31)
  • 1000 TABLET, FILM COATED in 1 BOTTLE (62332-319-91)
source: ndc

Packages (3)

62332-319-30 30 TABLET, FILM COATED in 1 BOTTLE (62332-319-30) 62332-319-31 100 TABLET, FILM COATED in 1 BOTTLE (62332-319-31) 62332-319-91 1000 TABLET, FILM COATED in 1 BOTTLE (62332-319-91)

Ingredients (1)

desipramine hydrochloride (100 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": "06c52509-29c8-41c5-8492-3458df75f3d5", "openfda": {"upc": ["0362332320318"], "unii": ["1Y58DO4MY1"], "rxcui": ["1099288", "1099292", "1099296", "1099300", "1099304", "1099316"], "spl_set_id": ["cad14805-64d8-4257-b5f1-d56e0063f0e2"], "manufacturer_name": ["Alembic Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (62332-319-30)", "package_ndc": "62332-319-30", "marketing_start_date": "20210708"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (62332-319-31)", "package_ndc": "62332-319-31", "marketing_start_date": "20210708"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (62332-319-91)", "package_ndc": "62332-319-91", "marketing_start_date": "20210708"}], "brand_name": "DESIPRAMINE HYDROCHLORIDE", "product_id": "62332-319_06c52509-29c8-41c5-8492-3458df75f3d5", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "62332-319", "generic_name": "DESIPRAMINE HYDROCHLORIDE", "labeler_name": "Alembic Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DESIPRAMINE HYDROCHLORIDE", "active_ingredients": [{"name": "DESIPRAMINE HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA209785", "marketing_category": "ANDA", "marketing_start_date": "20210708", "listing_expiration_date": "20261231"}