desipramine hydrochloride
Generic: desipramine hydrochloride
Labeler: actavis pharma, inc.Drug Facts
Product Profile
Brand Name
desipramine hydrochloride
Generic Name
desipramine hydrochloride
Labeler
actavis pharma, inc.
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
desipramine hydrochloride 75 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
45963-344
Product ID
45963-344_cb512a98-31c9-4ae9-9cc9-1d102302cfea
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA071602
Listing Expiration
2026-12-31
Marketing Start
2006-05-08
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
45963344
Hyphenated Format
45963-344
Supplemental Identifiers
RxCUI
UPC
UNII
Packaging Origin
Original Packager
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
ANDA071602 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 75 mg/1
Packaging
- 100 TABLET, FILM COATED in 1 BOTTLE (45963-344-02)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "cb512a98-31c9-4ae9-9cc9-1d102302cfea", "openfda": {"upc": ["0345963345028", "0345963346506", "0345963344021", "0345963343024", "0345963341020"], "unii": ["1Y58DO4MY1"], "rxcui": ["1099288", "1099292", "1099296", "1099300", "1099304", "1099316"], "spl_set_id": ["ba02a95d-d82e-4a13-90b4-a219abc0249a"], "manufacturer_name": ["Actavis Pharma, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (45963-344-02)", "package_ndc": "45963-344-02", "marketing_start_date": "20060508"}], "brand_name": "Desipramine Hydrochloride", "product_id": "45963-344_cb512a98-31c9-4ae9-9cc9-1d102302cfea", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "45963-344", "generic_name": "Desipramine Hydrochloride", "labeler_name": "Actavis Pharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Desipramine Hydrochloride", "active_ingredients": [{"name": "DESIPRAMINE HYDROCHLORIDE", "strength": "75 mg/1"}], "application_number": "ANDA071602", "marketing_category": "ANDA", "marketing_start_date": "20060508", "listing_expiration_date": "20261231"}