imipramine hydrochloride

Generic: imipramine hydrochloride

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name imipramine hydrochloride
Generic Name imipramine hydrochloride
Labeler proficient rx lp
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

imipramine hydrochloride 10 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 71205-804
Product ID 71205-804_3f90b8dd-7234-4428-b896-943d052dd05f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA040903
Listing Expiration 2026-12-31
Marketing Start 2016-04-07

Pharmacologic Class

Classes
tricyclic antidepressant [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 71205804
Hyphenated Format 71205-804

Supplemental Identifiers

RxCUI
835593
UPC
0371205804305
UNII
BKE5Q1J60U

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 imipramine hydrochloride (source: ndc)
Generic Name imipramine hydrochloride (source: ndc)
Application Number ANDA040903 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (71205-804-30)
  • 60 TABLET, FILM COATED in 1 BOTTLE (71205-804-60)
  • 90 TABLET, FILM COATED in 1 BOTTLE (71205-804-90)
source: ndc

Packages (3)

71205-804-30 30 TABLET, FILM COATED in 1 BOTTLE (71205-804-30) 71205-804-60 60 TABLET, FILM COATED in 1 BOTTLE (71205-804-60) 71205-804-90 90 TABLET, FILM COATED in 1 BOTTLE (71205-804-90)

Ingredients (1)

imipramine hydrochloride (10 mg/1)

Linked Drug Pages (1)

Imipramine Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3f90b8dd-7234-4428-b896-943d052dd05f", "openfda": {"upc": ["0371205804305"], "unii": ["BKE5Q1J60U"], "rxcui": ["835593"], "spl_set_id": ["3f90b8dd-7234-4428-b896-943d052dd05f"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71205-804-30)", "package_ndc": "71205-804-30", "marketing_start_date": "20230605"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71205-804-60)", "package_ndc": "71205-804-60", "marketing_start_date": "20230605"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71205-804-90)", "package_ndc": "71205-804-90", "marketing_start_date": "20230605"}], "brand_name": "Imipramine Hydrochloride", "product_id": "71205-804_3f90b8dd-7234-4428-b896-943d052dd05f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "71205-804", "generic_name": "Imipramine Hydrochloride", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Imipramine Hydrochloride", "active_ingredients": [{"name": "IMIPRAMINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA040903", "marketing_category": "ANDA", "marketing_start_date": "20160407", "listing_expiration_date": "20261231"}