Package 57664-690-88

Brand: amitriptyline hydrochloride

Generic: amitriptyline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 57664-690-88
Digits Only 5766469088
Product NDC 57664-690
Product ID 57664-690_326a1cd7-1376-8b5e-e063-6294a90a80aa
Description

100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (57664-690-88)

Marketing

Marketing Status
Marketed Since 1987-07-14
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": "326a1cd7-1376-8b5e-e063-6294a90a80aa", "openfda": {"upc": ["0357664689882", "0357664691885", "0357664687888", "0357664690888", "0357664688885", "0357664692882"], "unii": ["26LUD4JO9K"], "rxcui": ["856762", "856773", "856783", "856834", "856845", "856853"], "spl_set_id": ["4e520c63-1cf6-40f6-a51c-3f9b0e181342"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (57664-690-88)", "package_ndc": "57664-690-88", "marketing_start_date": "19870714"}], "brand_name": "Amitriptyline Hydrochloride", "product_id": "57664-690_326a1cd7-1376-8b5e-e063-6294a90a80aa", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "57664-690", "generic_name": "Amitriptyline Hydrochloride", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amitriptyline Hydrochloride", "active_ingredients": [{"name": "AMITRIPTYLINE HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA089399", "marketing_category": "ANDA", "marketing_start_date": "19870714", "listing_expiration_date": "20261231"}