Package 10702-006-10

Brand: cyclobenzaprine hydrochloride

Generic: cyclobenzaprine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 10702-006-10
Digits Only 1070200610
Product NDC 10702-006
Product ID 10702-006_7d541fa9-d74b-5236-e053-2991aa0acc0e
Description

1000 TABLET, FILM COATED in 1 BOTTLE (10702-006-10)

Marketing

Marketing Status
Marketed Since 2014-07-31
Brand cyclobenzaprine hydrochloride
Generic cyclobenzaprine hydrochloride
Sample Package No

Linked Drug Pages (1)

Cyclobenzaprine Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "7d541fa9-d74b-5236-e053-2991aa0acc0e", "openfda": {"unii": ["0VE05JYS2P"], "rxcui": ["828320", "828348"], "spl_set_id": ["5b756c04-e7b8-4efe-815a-3f3e020727fb"], "manufacturer_name": ["KVK-TECH, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (10702-006-01)", "package_ndc": "10702-006-01", "marketing_start_date": "20140731"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (10702-006-10)", "package_ndc": "10702-006-10", "marketing_start_date": "20140731"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (10702-006-50)", "package_ndc": "10702-006-50", "marketing_start_date": "20140731"}], "brand_name": "Cyclobenzaprine Hydrochloride", "product_id": "10702-006_7d541fa9-d74b-5236-e053-2991aa0acc0e", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "10702-006", "generic_name": "Cyclobenzaprine Hydrochloride", "labeler_name": "KVK-TECH, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cyclobenzaprine Hydrochloride", "active_ingredients": [{"name": "CYCLOBENZAPRINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA078048", "marketing_category": "ANDA", "marketing_start_date": "20140731", "listing_expiration_date": "20261231"}