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
Routes
ORAL
Active Ingredients

imipramine hydrochloride 10 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 82804-956
Product ID 82804-956_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 82804956
Hyphenated Format 82804-956

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
  • 10 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (82804-956-00)
  • 1000 TABLET in 1 BOTTLE (82804-956-11)
  • 30 TABLET in 1 BOTTLE (82804-956-30)
  • 500 TABLET in 1 BOTTLE (82804-956-55)
  • 60 TABLET in 1 BOTTLE (82804-956-60)
  • 120 TABLET in 1 BOTTLE (82804-956-72)
  • 90 TABLET in 1 BOTTLE (82804-956-90)
source: ndc

Packages (7)

Ingredients (1)

imipramine hydrochloride (10 mg/1)

Linked Drug Pages (1)

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 (82804-956-00)", "package_ndc": "82804-956-00", "marketing_start_date": "20260112"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (82804-956-11)", "package_ndc": "82804-956-11", "marketing_start_date": "20260112"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (82804-956-30)", "package_ndc": "82804-956-30", "marketing_start_date": "20260112"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (82804-956-55)", "package_ndc": "82804-956-55", "marketing_start_date": "20260112"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (82804-956-60)", "package_ndc": "82804-956-60", "marketing_start_date": "20260112"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE (82804-956-72)", "package_ndc": "82804-956-72", "marketing_start_date": "20260112"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (82804-956-90)", "package_ndc": "82804-956-90", "marketing_start_date": "20260112"}], "brand_name": "Imipramine Hydrochloride", "product_id": "82804-956_5997822f-ce83-4091-be71-21a6b01caaba", "dosage_form": "TABLET", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "82804-956", "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": "ANDA040751", "marketing_category": "ANDA", "marketing_start_date": "20200801", "listing_expiration_date": "20271231"}