Package 0781-1486-10
Brand: amitriptyline hydrochloride
Generic: amitriptyline hydrochloridePackage Facts
Identity
Package NDC
0781-1486-10
Digits Only
0781148610
Product NDC
0781-1486
Description
1000 TABLET, FILM COATED in 1 BOTTLE (0781-1486-10)
Marketing
Marketing Status
Brand
amitriptyline hydrochloride
Generic
amitriptyline hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "9df45420-7268-454e-9624-8da48c97b7db", "openfda": {"unii": ["26LUD4JO9K"], "rxcui": ["856762", "856773", "856783", "856834", "856845", "856853"], "spl_set_id": ["705a2bae-031d-4218-82fe-4346542c0baa"], "manufacturer_name": ["Sandoz Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (0781-1486-01)", "package_ndc": "0781-1486-01", "marketing_start_date": "19771121"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (0781-1486-10)", "package_ndc": "0781-1486-10", "marketing_start_date": "19771121"}], "brand_name": "Amitriptyline Hydrochloride", "product_id": "0781-1486_9df45420-7268-454e-9624-8da48c97b7db", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "0781-1486", "generic_name": "Amitriptyline Hydrochloride", "labeler_name": "Sandoz Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amitriptyline Hydrochloride", "active_ingredients": [{"name": "AMITRIPTYLINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA085968", "marketing_category": "ANDA", "marketing_start_date": "19771121", "listing_expiration_date": "20261231"}