Package 0406-9906-03

Brand: anafranil

Generic: clomipramine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0406-9906-03
Digits Only 0406990603
Product NDC 0406-9906
Description

30 CAPSULE in 1 BOTTLE (0406-9906-03)

Marketing

Marketing Status
Marketed Since 1989-12-29
Brand anafranil
Generic clomipramine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "07af3867-7f3e-4e1c-8100-ad276cb6185f", "openfda": {"upc": ["0304069908032", "0304069906038", "0304069907035"], "unii": ["2LXW0L6GWJ"], "rxcui": ["857297", "857299", "857301", "857303", "857305", "857307"], "spl_set_id": ["4074b555-7635-41a9-809d-fae3b3610059"], "manufacturer_name": ["SpecGx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (0406-9906-03)", "package_ndc": "0406-9906-03", "marketing_start_date": "19891229"}], "brand_name": "ANAFRANIL", "product_id": "0406-9906_07af3867-7f3e-4e1c-8100-ad276cb6185f", "dosage_form": "CAPSULE", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "0406-9906", "generic_name": "clomipramine hydrochloride", "labeler_name": "SpecGx LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ANAFRANIL", "active_ingredients": [{"name": "CLOMIPRAMINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "NDA019906", "marketing_category": "NDA", "marketing_start_date": "19891229", "listing_expiration_date": "20261231"}