desipramine hydrochloride

Generic: desipramine hydrochloride

Labeler: heritage pharmaceuticals inc. d/b/a avet pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name desipramine hydrochloride
Generic Name desipramine hydrochloride
Labeler heritage pharmaceuticals inc. d/b/a avet pharmaceuticals inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

desipramine hydrochloride 75 mg/1

Manufacturer
Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 23155-581
Product ID 23155-581_49984729-ddde-44ed-927b-8a4ba65cefa0
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA207433
Marketing Start 2016-11-01
Marketing End 2027-03-31

Pharmacologic Class

Classes
tricyclic antidepressant [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 23155581
Hyphenated Format 23155-581

Supplemental Identifiers

RxCUI
1099288 1099292 1099296 1099300 1099304 1099316
UPC
0323155579017 0323155582017 0323155578010 0323155583250 0323155581010 0323155580013
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 ANDA207433 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 75 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (23155-581-01)
source: ndc

Packages (1)

23155-581-01 100 TABLET in 1 BOTTLE (23155-581-01)

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": "49984729-ddde-44ed-927b-8a4ba65cefa0", "openfda": {"upc": ["0323155579017", "0323155582017", "0323155578010", "0323155583250", "0323155581010", "0323155580013"], "unii": ["1Y58DO4MY1"], "rxcui": ["1099288", "1099292", "1099296", "1099300", "1099304", "1099316"], "spl_set_id": ["ee14dd2c-c54b-4cd1-a3a0-f7ad5a5a0ed0"], "manufacturer_name": ["Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (23155-581-01)", "package_ndc": "23155-581-01", "marketing_end_date": "20270331", "marketing_start_date": "20161101"}], "brand_name": "DESIPRAMINE HYDROCHLORIDE", "product_id": "23155-581_49984729-ddde-44ed-927b-8a4ba65cefa0", "dosage_form": "TABLET", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "23155-581", "generic_name": "desipramine hydrochloride", "labeler_name": "Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DESIPRAMINE HYDROCHLORIDE", "active_ingredients": [{"name": "DESIPRAMINE HYDROCHLORIDE", "strength": "75 mg/1"}], "application_number": "ANDA207433", "marketing_category": "ANDA", "marketing_end_date": "20270331", "marketing_start_date": "20161101"}