desipramine hcl

Generic: desipramine hcl

Labeler: direct_rx
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name desipramine hcl
Generic Name desipramine hcl
Labeler direct_rx
Dosage Form TABLET
Routes
ORAL
Active Ingredients

desipramine hydrochloride 10 mg/1

Manufacturer
Direct_Rx

Identifiers & Regulatory

Product NDC 72189-391
Product ID 72189-391_2c4cdf7a-45d8-784b-e063-6294a90a82b9
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA204963
Listing Expiration 2026-12-31
Marketing Start 2022-11-16

Pharmacologic Class

Classes
tricyclic antidepressant [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72189391
Hyphenated Format 72189-391

Supplemental Identifiers

RxCUI
1099288
UNII
1Y58DO4MY1

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 hcl (source: ndc)
Generic Name desipramine hcl (source: ndc)
Application Number ANDA204963 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (72189-391-30)
source: ndc

Packages (1)

72189-391-30 30 TABLET in 1 BOTTLE (72189-391-30)

Ingredients (1)

desipramine hydrochloride (10 mg/1)

Linked Drug Pages (1)

Desipramine HCL ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2c4cdf7a-45d8-784b-e063-6294a90a82b9", "openfda": {"unii": ["1Y58DO4MY1"], "rxcui": ["1099288"], "spl_set_id": ["ed9d2290-9ad9-ecff-e053-2a95a90a5fd6"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (72189-391-30)", "package_ndc": "72189-391-30", "marketing_start_date": "20221116"}], "brand_name": "Desipramine HCL", "product_id": "72189-391_2c4cdf7a-45d8-784b-e063-6294a90a82b9", "dosage_form": "TABLET", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "72189-391", "generic_name": "Desipramine HCL", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Desipramine HCL", "active_ingredients": [{"name": "DESIPRAMINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA204963", "marketing_category": "ANDA", "marketing_start_date": "20221116", "listing_expiration_date": "20261231"}