clomipramine hydrochloride

Generic: clomipramine hydrochloride

Labeler: micro labs limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name clomipramine hydrochloride
Generic Name clomipramine hydrochloride
Labeler micro labs limited
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

clomipramine hydrochloride 50 mg/1

Manufacturer
Micro Labs Limited

Identifiers & Regulatory

Product NDC 42571-343
Product ID 42571-343_35016ce5-40f8-fce9-e063-6394a90af976
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA213219
Listing Expiration 2026-12-31
Marketing Start 2020-09-01

Pharmacologic Class

Classes
tricyclic antidepressant [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 42571343
Hyphenated Format 42571-343

Supplemental Identifiers

RxCUI
857297 857301 857305
UPC
0342571342302 0342571344306 0342571343309
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 ANDA213219 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 100 CAPSULE in 1 BOTTLE (42571-343-01)
  • 30 CAPSULE in 1 BOTTLE (42571-343-30)
  • 90 CAPSULE in 1 BOTTLE (42571-343-90)
source: ndc

Packages (3)

Ingredients (1)

clomipramine hydrochloride (50 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "35016ce5-40f8-fce9-e063-6394a90af976", "openfda": {"upc": ["0342571342302", "0342571344306", "0342571343309"], "unii": ["2LXW0L6GWJ"], "rxcui": ["857297", "857301", "857305"], "spl_set_id": ["0bbee292-0fba-4606-9c8e-4723742682c0"], "manufacturer_name": ["Micro Labs Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (42571-343-01)", "package_ndc": "42571-343-01", "marketing_start_date": "20200901"}, {"sample": false, "description": "30 CAPSULE in 1 BOTTLE (42571-343-30)", "package_ndc": "42571-343-30", "marketing_start_date": "20200901"}, {"sample": false, "description": "90 CAPSULE in 1 BOTTLE (42571-343-90)", "package_ndc": "42571-343-90", "marketing_start_date": "20200901"}], "brand_name": "CLOMIPRAMINE HYDROCHLORIDE", "product_id": "42571-343_35016ce5-40f8-fce9-e063-6394a90af976", "dosage_form": "CAPSULE", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "42571-343", "generic_name": "CLOMIPRAMINE HYDROCHLORIDE", "labeler_name": "Micro Labs Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CLOMIPRAMINE HYDROCHLORIDE", "active_ingredients": [{"name": "CLOMIPRAMINE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA213219", "marketing_category": "ANDA", "marketing_start_date": "20200901", "listing_expiration_date": "20261231"}