clomipramine hydrochloride
Generic: clomipramine hydrochloride
Labeler: specgx llcDrug Facts
Product Profile
Brand Name
clomipramine hydrochloride
Generic Name
clomipramine hydrochloride
Labeler
specgx llc
Dosage Form
CAPSULE
Routes
Active Ingredients
clomipramine hydrochloride 50 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
0406-8807
Product ID
0406-8807_f7da2c91-cd58-46c3-b716-846a454cfb07
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA019906
Listing Expiration
2026-12-31
Marketing Start
2015-06-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
04068807
Hyphenated Format
0406-8807
Supplemental Identifiers
RxCUI
UPC
UNII
Packaging Origin
Original Packager
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
NDA019906 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 50 mg/1
Packaging
- 100 CAPSULE in 1 BOTTLE (0406-8807-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "f7da2c91-cd58-46c3-b716-846a454cfb07", "openfda": {"upc": ["0304068808012", "0304068807015", "0304068806018"], "unii": ["2LXW0L6GWJ"], "rxcui": ["857297", "857301", "857305"], "spl_set_id": ["d7cee3fa-d05c-4702-8f75-f446627bdb49"], "manufacturer_name": ["SpecGx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (0406-8807-01)", "package_ndc": "0406-8807-01", "marketing_start_date": "20150601"}], "brand_name": "CLOMIPRAMINE HYDROCHLORIDE", "product_id": "0406-8807_f7da2c91-cd58-46c3-b716-846a454cfb07", "dosage_form": "CAPSULE", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "0406-8807", "generic_name": "clomipramine hydrochloride", "labeler_name": "SpecGx LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CLOMIPRAMINE HYDROCHLORIDE", "active_ingredients": [{"name": "CLOMIPRAMINE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "NDA019906", "marketing_category": "NDA", "marketing_start_date": "20150601", "listing_expiration_date": "20261231"}