imipramine hydrochloride

Generic: imipramine hydrochloride

Labeler: remedyrepack inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name imipramine hydrochloride
Generic Name imipramine hydrochloride
Labeler remedyrepack inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

imipramine hydrochloride 25 mg/1

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-3526
Product ID 70518-3526_3f14b9c9-5d0e-d2ec-e063-6294a90a6815
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA040751
Listing Expiration 2026-12-31
Marketing Start 2020-09-19

Pharmacologic Class

Classes
tricyclic antidepressant [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 705183526
Hyphenated Format 70518-3526

Supplemental Identifiers

RxCUI
835564
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
  • 30 TABLET in 1 BLISTER PACK (70518-3526-0)
source: ndc

Packages (1)

70518-3526-0 30 TABLET in 1 BLISTER PACK (70518-3526-0)

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": "3f14b9c9-5d0e-d2ec-e063-6294a90a6815", "openfda": {"unii": ["BKE5Q1J60U"], "rxcui": ["835564"], "spl_set_id": ["02c19a0a-3d9d-4881-ad14-1687aafd87b5"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-3526-0)", "package_ndc": "70518-3526-0", "marketing_start_date": "20200919"}], "brand_name": "Imipramine Hydrochloride", "product_id": "70518-3526_3f14b9c9-5d0e-d2ec-e063-6294a90a6815", "dosage_form": "TABLET", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "70518-3526", "generic_name": "Imipramine Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "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": "20200919", "listing_expiration_date": "20261231"}