Package 0093-3420-01

Brand: cyclobenzaprine hydrochloride

Generic: cyclobenzaprine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0093-3420-01
Digits Only 0093342001
Product NDC 0093-3420
Product ID 0093-3420_43707f11-5cf5-46a1-af67-c12153c11fd1
Description

100 TABLET, FILM COATED in 1 BOTTLE (0093-3420-01)

Marketing

Marketing Status
Marketed Since 2021-07-20
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": "43707f11-5cf5-46a1-af67-c12153c11fd1", "openfda": {"upc": ["0300933421010", "0300933422017", "0300933420013"], "unii": ["0VE05JYS2P"], "rxcui": ["828299", "828320", "828348"], "spl_set_id": ["1d9e34cc-eee9-4147-abf8-c810a80e39d2"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (0093-3420-01)", "package_ndc": "0093-3420-01", "marketing_start_date": "20210720"}], "brand_name": "Cyclobenzaprine Hydrochloride", "product_id": "0093-3420_43707f11-5cf5-46a1-af67-c12153c11fd1", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "0093-3420", "generic_name": "Cyclobenzaprine Hydrochloride", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cyclobenzaprine Hydrochloride", "active_ingredients": [{"name": "CYCLOBENZAPRINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA071611", "marketing_category": "ANDA", "marketing_start_date": "20210720", "listing_expiration_date": "20271231"}