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, FILM COATED
Routes
ORAL
Active Ingredients

imipramine hydrochloride 50 mg/1

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-1588
Product ID 70518-1588_494e4586-13e0-bc7a-e063-6294a90a90cb
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA040903
Listing Expiration 2027-12-31
Marketing Start 2018-10-25

Pharmacologic Class

Classes
tricyclic antidepressant [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 705181588
Hyphenated Format 70518-1588

Supplemental Identifiers

RxCUI
835568
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
  • 50 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1588-0)
source: ndc

Packages (1)

70518-1588-0 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1588-0)

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": "494e4586-13e0-bc7a-e063-6294a90a90cb", "openfda": {"unii": ["BKE5Q1J60U"], "rxcui": ["835568"], "spl_set_id": ["db007ac0-020e-4962-8903-7497ab96a74e"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1588-0)", "package_ndc": "70518-1588-0", "marketing_start_date": "20181025"}], "brand_name": "Imipramine Hydrochloride", "product_id": "70518-1588_494e4586-13e0-bc7a-e063-6294a90a90cb", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "70518-1588", "generic_name": "Imipramine Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Imipramine Hydrochloride", "active_ingredients": [{"name": "IMIPRAMINE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA040903", "marketing_category": "ANDA", "marketing_start_date": "20181025", "listing_expiration_date": "20271231"}