clomipramine hydrochloride
Generic: clomipramine hydrochloride
Labeler: major pharmaceuticalsDrug Facts
Product Profile
Brand Name
clomipramine hydrochloride
Generic Name
clomipramine hydrochloride
Labeler
major pharmaceuticals
Dosage Form
CAPSULE
Routes
Active Ingredients
clomipramine hydrochloride 25 mg/1
Manufacturer
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
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
09047038
Hyphenated Format
0904-7038
Supplemental Identifiers
RxCUI
UNII
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
source: ndc
Resolved Composition
Strengths
- 25 mg/1
Packaging
- 30 BLISTER PACK in 1 CARTON (0904-7038-07) / 1 CAPSULE in 1 BLISTER PACK
Packages (1)
Ingredients (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"}