desipramine hydrochloride

Generic: desipramine hydrochloride

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

Drug Facts

Product Profile

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

desipramine hydrochloride 25 mg/1

Manufacturer
Alembic Pharmaceuticals Limited

Identifiers & Regulatory

Product NDC 46708-316
Product ID 46708-316_878a2586-20af-4f35-8908-82474cc732a3
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 46708316
Hyphenated Format 46708-316

Supplemental Identifiers

RxCUI
1099288 1099292 1099296 1099300 1099304 1099316
UPC
0346708315306
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
  • 25 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (46708-316-30)
  • 100 TABLET, FILM COATED in 1 BOTTLE (46708-316-31)
  • 1000 TABLET, FILM COATED in 1 BOTTLE (46708-316-91)
source: ndc

Packages (3)

46708-316-30 30 TABLET, FILM COATED in 1 BOTTLE (46708-316-30) 46708-316-31 100 TABLET, FILM COATED in 1 BOTTLE (46708-316-31) 46708-316-91 1000 TABLET, FILM COATED in 1 BOTTLE (46708-316-91)

Ingredients (1)

desipramine hydrochloride (25 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": "878a2586-20af-4f35-8908-82474cc732a3", "openfda": {"upc": ["0346708315306"], "unii": ["1Y58DO4MY1"], "rxcui": ["1099288", "1099292", "1099296", "1099300", "1099304", "1099316"], "spl_set_id": ["8b6d2289-aac9-4007-a73d-c168fd2e1d9e"], "manufacturer_name": ["Alembic Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (46708-316-30)", "package_ndc": "46708-316-30", "marketing_start_date": "20210708"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (46708-316-31)", "package_ndc": "46708-316-31", "marketing_start_date": "20210708"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (46708-316-91)", "package_ndc": "46708-316-91", "marketing_start_date": "20210708"}], "brand_name": "DESIPRAMINE HYDROCHLORIDE", "product_id": "46708-316_878a2586-20af-4f35-8908-82474cc732a3", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "46708-316", "generic_name": "DESIPRAMINE HYDROCHLORIDE", "labeler_name": "Alembic Pharmaceuticals Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DESIPRAMINE HYDROCHLORIDE", "active_ingredients": [{"name": "DESIPRAMINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA209785", "marketing_category": "ANDA", "marketing_start_date": "20210708", "listing_expiration_date": "20261231"}