clomipramine hydrochloride

Generic: clomipramine hydrochloride

Labeler: sun pharmaceutical industries, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name clomipramine hydrochloride
Generic Name clomipramine hydrochloride
Labeler sun pharmaceutical industries, inc.
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

clomipramine hydrochloride 75 mg/1

Manufacturer
Sun Pharmaceutical Industries, Inc.

Identifiers & Regulatory

Product NDC 51672-4013
Product ID 51672-4013_34699b9e-d070-64b2-e063-6294a90a0f6d
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 516724013
Hyphenated Format 51672-4013

Supplemental Identifiers

RxCUI
857297 857301 857305
UNII
2LXW0L6GWJ

Packaging Origin

Original Packager
true

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
  • 75 mg/1
source: ndc
Packaging
  • 100 CAPSULE in 1 BOTTLE (51672-4013-1)
  • 60 CAPSULE in 1 BOTTLE (51672-4013-4)
  • 90 CAPSULE in 1 BOTTLE (51672-4013-5)
  • 30 CAPSULE in 1 BOTTLE (51672-4013-6)
source: ndc

Packages (4)

51672-4013-1 100 CAPSULE in 1 BOTTLE (51672-4013-1) 51672-4013-4 60 CAPSULE in 1 BOTTLE (51672-4013-4) 51672-4013-5 90 CAPSULE in 1 BOTTLE (51672-4013-5) 51672-4013-6 30 CAPSULE in 1 BOTTLE (51672-4013-6)

Ingredients (1)

clomipramine hydrochloride (75 mg/1)

Linked Drug Pages (1)

CLOMIPRAMINE HYDROCHLORIDE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "34699b9e-d070-64b2-e063-6294a90a0f6d", "openfda": {"unii": ["2LXW0L6GWJ"], "rxcui": ["857297", "857301", "857305"], "spl_set_id": ["db752dbd-be41-4cdd-8a13-ed1ff9ef7461"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (51672-4013-1)", "package_ndc": "51672-4013-1", "marketing_start_date": "19961231"}, {"sample": false, "description": "60 CAPSULE in 1 BOTTLE (51672-4013-4)", "package_ndc": "51672-4013-4", "marketing_start_date": "19961231"}, {"sample": false, "description": "90 CAPSULE in 1 BOTTLE (51672-4013-5)", "package_ndc": "51672-4013-5", "marketing_start_date": "19961231"}, {"sample": false, "description": "30 CAPSULE in 1 BOTTLE (51672-4013-6)", "package_ndc": "51672-4013-6", "marketing_start_date": "19961231"}], "brand_name": "CLOMIPRAMINE HYDROCHLORIDE", "product_id": "51672-4013_34699b9e-d070-64b2-e063-6294a90a0f6d", "dosage_form": "CAPSULE", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "51672-4013", "generic_name": "Clomipramine Hydrochloride", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CLOMIPRAMINE HYDROCHLORIDE", "active_ingredients": [{"name": "CLOMIPRAMINE HYDROCHLORIDE", "strength": "75 mg/1"}], "application_number": "ANDA074694", "marketing_category": "ANDA", "marketing_start_date": "19961231", "listing_expiration_date": "20261231"}