Package 60760-212-15

Brand: amitriptyline hydrochloride

Generic: amitriptyline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 60760-212-15
Digits Only 6076021215
Product NDC 60760-212
Product ID 60760-212_0c05b1cc-f9ef-1af0-e063-6294a90aea2b
Description

15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-212-15)

Marketing

Marketing Status
Marketed Since 2016-02-26
Brand amitriptyline hydrochloride
Generic amitriptyline hydrochloride
Sample Package No

Linked Drug Pages (1)

AMITRIPTYLINE HYDROCHLORIDE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "0c05b1cc-f9ef-1af0-e063-6294a90aea2b", "openfda": {"unii": ["26LUD4JO9K"], "rxcui": ["856783"], "spl_set_id": ["60a4fa41-bf0b-7ea4-e053-2991aa0a0cd0"], "manufacturer_name": ["St. Mary's Medical Park Pharmacy"]}, "finished": true, "packaging": [{"sample": false, "description": "15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-212-15)", "package_ndc": "60760-212-15", "marketing_start_date": "20160226"}], "brand_name": "AMITRIPTYLINE HYDROCHLORIDE", "product_id": "60760-212_0c05b1cc-f9ef-1af0-e063-6294a90aea2b", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "60760-212", "generic_name": "AMITRIPTYLINE HYDROCHLORIDE", "labeler_name": "St. Mary's Medical Park Pharmacy", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "AMITRIPTYLINE HYDROCHLORIDE", "active_ingredients": [{"name": "AMITRIPTYLINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA202446", "marketing_category": "ANDA", "marketing_start_date": "20160226", "listing_expiration_date": "20261231"}