clomipramine hydrochloride

Generic: clomipramine hydrochloride

Labeler: major pharmaceuticals
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name clomipramine hydrochloride
Generic Name clomipramine hydrochloride
Labeler major pharmaceuticals
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

clomipramine hydrochloride 25 mg/1

Manufacturer
Major Pharmaceuticals

Identifiers & Regulatory

Product NDC 0904-7038
Product ID 0904-7038_b7641ab7-974c-4814-97ba-44cf2ca7e10f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA074694
Listing Expiration 2026-12-31
Marketing Start 1996-12-31

Pharmacologic Class

Classes
tricyclic antidepressant [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 09047038
Hyphenated Format 0904-7038

Supplemental Identifiers

RxCUI
857297 857301
UNII
2LXW0L6GWJ

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 clomipramine hydrochloride (source: ndc)
Generic Name clomipramine hydrochloride (source: ndc)
Application Number ANDA074694 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 30 BLISTER PACK in 1 CARTON (0904-7038-07) / 1 CAPSULE in 1 BLISTER PACK
source: ndc

Packages (1)

Ingredients (1)

clomipramine hydrochloride (25 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "b7641ab7-974c-4814-97ba-44cf2ca7e10f", "openfda": {"unii": ["2LXW0L6GWJ"], "rxcui": ["857297", "857301"], "spl_set_id": ["eff91018-5a5e-4426-96ae-71ecd82273b7"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "30 BLISTER PACK in 1 CARTON (0904-7038-07)  / 1 CAPSULE in 1 BLISTER PACK", "package_ndc": "0904-7038-07", "marketing_start_date": "19961231"}], "brand_name": "CLOMIPRAMINE HYDROCHLORIDE", "product_id": "0904-7038_b7641ab7-974c-4814-97ba-44cf2ca7e10f", "dosage_form": "CAPSULE", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "0904-7038", "generic_name": "Clomipramine Hydrochloride", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CLOMIPRAMINE HYDROCHLORIDE", "active_ingredients": [{"name": "CLOMIPRAMINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA074694", "marketing_category": "ANDA", "marketing_start_date": "19961231", "listing_expiration_date": "20261231"}