desipramine hydrochloride

Generic: desipramine hydrochloride

Labeler: chartwell rx, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name desipramine hydrochloride
Generic Name desipramine hydrochloride
Labeler chartwell rx, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

desipramine hydrochloride 25 mg/1

Manufacturer
Chartwell RX, LLC

Identifiers & Regulatory

Product NDC 62135-594
Product ID 62135-594_45895d97-14b1-1beb-e063-6394a90a2930
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA207433
Listing Expiration 2026-12-31
Marketing Start 2016-11-01

Pharmacologic Class

Classes
tricyclic antidepressant [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 62135594
Hyphenated Format 62135-594

Supplemental Identifiers

RxCUI
1099288 1099292 1099296 1099300 1099304 1099316
UPC
0362135599300 0362135593124 0362135597122 0362135598303 0362135594121 0362135595128
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
  • 25 mg/1
source: ndc
Packaging
  • 120 TABLET in 1 BOTTLE (62135-594-12)
source: ndc

Packages (1)

62135-594-12 120 TABLET in 1 BOTTLE (62135-594-12)

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": "45895d97-14b1-1beb-e063-6394a90a2930", "openfda": {"upc": ["0362135599300", "0362135593124", "0362135597122", "0362135598303", "0362135594121", "0362135595128"], "unii": ["1Y58DO4MY1"], "rxcui": ["1099288", "1099292", "1099296", "1099300", "1099304", "1099316"], "spl_set_id": ["6ab5e113-82ef-493d-a4e3-a2756608fa60"], "manufacturer_name": ["Chartwell RX, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "120 TABLET in 1 BOTTLE (62135-594-12)", "package_ndc": "62135-594-12", "marketing_start_date": "20230512"}], "brand_name": "Desipramine Hydrochloride", "product_id": "62135-594_45895d97-14b1-1beb-e063-6394a90a2930", "dosage_form": "TABLET", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "62135-594", "generic_name": "Desipramine Hydrochloride", "labeler_name": "Chartwell RX, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Desipramine Hydrochloride", "active_ingredients": [{"name": "DESIPRAMINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA207433", "marketing_category": "ANDA", "marketing_start_date": "20161101", "listing_expiration_date": "20261231"}