imipramine hydrochloride (82804-957)

Drug Facts

Product Profile

Brand Name imipramine hydrochloride

Generic Name imipramine hydrochloride

Labeler proficient rx lp

Dosage Form TABLET

Routes

ORAL

Active Ingredients

imipramine hydrochloride 25 mg/1

Manufacturer

Proficient Rx LP

Identifiers & Regulatory

Product NDC 82804-957

Product ID 82804-957_5997822f-ce83-4091-be71-21a6b01caaba

Product Type HUMAN PRESCRIPTION DRUG

Marketing Category ANDA

Application Number ANDA040751

Listing Expiration 2027-12-31

Marketing Start 2020-08-01

Pharmacologic Class

Classes

tricyclic antidepressant [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 82804957

Hyphenated Format 82804-957

Supplemental Identifiers

RxCUI

835564 835568 835593

UPC

0382804957309 0382804956302 0382804958306

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 ANDA040751 (source: ndc)

Routes

ORAL

source: ndc

Resolved Composition

Strengths

25 mg/1

source: ndc

Packaging

100 TABLET in 1 BOTTLE (82804-957-00)
1000 TABLET in 1 BOTTLE (82804-957-11)
30 TABLET in 1 BOTTLE (82804-957-30)
500 TABLET in 1 BOTTLE (82804-957-55)
60 TABLET in 1 BOTTLE (82804-957-60)
120 TABLET in 1 BOTTLE (82804-957-72)
90 TABLET in 1 BOTTLE (82804-957-90)

source: ndc

Packages (7)

82804-957-00 100 TABLET in 1 BOTTLE (82804-957-00) 82804-957-11 1000 TABLET in 1 BOTTLE (82804-957-11) 82804-957-30 30 TABLET in 1 BOTTLE (82804-957-30) 82804-957-55 500 TABLET in 1 BOTTLE (82804-957-55) 82804-957-60 60 TABLET in 1 BOTTLE (82804-957-60) 82804-957-72 120 TABLET in 1 BOTTLE (82804-957-72) 82804-957-90 90 TABLET in 1 BOTTLE (82804-957-90)

Ingredients (1)

imipramine hydrochloride (25 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": "5997822f-ce83-4091-be71-21a6b01caaba", "openfda": {"upc": ["0382804957309", "0382804956302", "0382804958306"], "unii": ["BKE5Q1J60U"], "rxcui": ["835564", "835568", "835593"], "spl_set_id": ["5997822f-ce83-4091-be71-21a6b01caaba"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (82804-957-00)", "package_ndc": "82804-957-00", "marketing_start_date": "20260112"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (82804-957-11)", "package_ndc": "82804-957-11", "marketing_start_date": "20260112"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (82804-957-30)", "package_ndc": "82804-957-30", "marketing_start_date": "20260112"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (82804-957-55)", "package_ndc": "82804-957-55", "marketing_start_date": "20260112"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (82804-957-60)", "package_ndc": "82804-957-60", "marketing_start_date": "20260112"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE (82804-957-72)", "package_ndc": "82804-957-72", "marketing_start_date": "20260112"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (82804-957-90)", "package_ndc": "82804-957-90", "marketing_start_date": "20260112"}], "brand_name": "Imipramine Hydrochloride", "product_id": "82804-957_5997822f-ce83-4091-be71-21a6b01caaba", "dosage_form": "TABLET", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "82804-957", "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": "25 mg/1"}], "application_number": "ANDA040751", "marketing_category": "ANDA", "marketing_start_date": "20200801", "listing_expiration_date": "20271231"}