imipramine hydrochloride

Generic: imipramine hydrochloride

Labeler: nucare pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name imipramine hydrochloride
Generic Name imipramine hydrochloride
Labeler nucare pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

imipramine hydrochloride 50 mg/1

Manufacturer
NuCare Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 68071-3669
Product ID 68071-3669_209ca50a-3b5e-3799-e063-6294a90a80e4
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA040751
Listing Expiration 2026-12-31
Marketing Start 2020-08-01

Pharmacologic Class

Classes
tricyclic antidepressant [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 680713669
Hyphenated Format 68071-3669

Supplemental Identifiers

RxCUI
835568
UPC
0368071366990
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
  • 50 mg/1
source: ndc
Packaging
  • 90 TABLET in 1 BOTTLE (68071-3669-9)
source: ndc

Packages (1)

68071-3669-9 90 TABLET in 1 BOTTLE (68071-3669-9)

Ingredients (1)

imipramine hydrochloride (50 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": "209ca50a-3b5e-3799-e063-6294a90a80e4", "openfda": {"upc": ["0368071366990"], "unii": ["BKE5Q1J60U"], "rxcui": ["835568"], "spl_set_id": ["209cc339-658a-577a-e063-6394a90a2b47"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (68071-3669-9)", "package_ndc": "68071-3669-9", "marketing_start_date": "20200801"}], "brand_name": "Imipramine Hydrochloride", "product_id": "68071-3669_209ca50a-3b5e-3799-e063-6294a90a80e4", "dosage_form": "TABLET", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "68071-3669", "generic_name": "Imipramine Hydrochloride", "labeler_name": "NuCare Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Imipramine Hydrochloride", "active_ingredients": [{"name": "IMIPRAMINE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA040751", "marketing_category": "ANDA", "marketing_start_date": "20200801", "listing_expiration_date": "20261231"}