Package 24979-035-04

Brand: cyclobenzaprine hydrochloride

Generic: cyclobenzaprine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 24979-035-04
Digits Only 2497903504
Product NDC 24979-035
Description

60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (24979-035-04)

Marketing

Marketing Status
Marketed Since 2019-03-01
Brand cyclobenzaprine hydrochloride
Generic cyclobenzaprine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "6d0e5e16-1e01-4ce6-9200-bdb5a651e923", "openfda": {"upc": ["0324979036045", "0324979035048"], "unii": ["0VE05JYS2P"], "rxcui": ["828353", "828358"], "spl_set_id": ["14f64ceb-ea5c-4d7c-a0c1-3f6a64847290"], "manufacturer_name": ["Upsher-Smith Laboratories, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (24979-035-04)", "package_ndc": "24979-035-04", "marketing_start_date": "20190301"}], "brand_name": "Cyclobenzaprine Hydrochloride", "product_id": "24979-035_6d0e5e16-1e01-4ce6-9200-bdb5a651e923", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "24979-035", "generic_name": "Cyclobenzaprine Hydrochloride", "labeler_name": "Upsher-Smith Laboratories, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cyclobenzaprine Hydrochloride", "active_ingredients": [{"name": "CYCLOBENZAPRINE HYDROCHLORIDE", "strength": "15 mg/1"}], "application_number": "ANDA091281", "marketing_category": "ANDA", "marketing_start_date": "20190301", "listing_expiration_date": "20261231"}