cyclobenzaprine hydrochloride
Generic: cyclobenzaprine
Labeler: ncs healthcare of ky, llc dba vangard labsDrug Facts
Product Profile
Brand Name
cyclobenzaprine hydrochloride
Generic Name
cyclobenzaprine
Labeler
ncs healthcare of ky, llc dba vangard labs
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
cyclobenzaprine hydrochloride 10 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
0615-8084
Product ID
0615-8084_3af92905-fa00-41fa-9156-037f58b21a0b
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA090478
Listing Expiration
2026-12-31
Marketing Start
2016-07-22
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
06158084
Hyphenated Format
0615-8084
Supplemental Identifiers
RxCUI
UNII
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
cyclobenzaprine hydrochloride (source: ndc)
Generic Name
cyclobenzaprine (source: ndc)
Application Number
ANDA090478 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/1
Packaging
- 15 TABLET, FILM COATED in 1 BLISTER PACK (0615-8084-05)
- 30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8084-39)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3af92905-fa00-41fa-9156-037f58b21a0b", "openfda": {"unii": ["0VE05JYS2P"], "rxcui": ["828348"], "spl_set_id": ["53688de9-2031-4d19-b422-4000285f7f47"], "manufacturer_name": ["NCS HealthCare of KY, LLC dba Vangard Labs"]}, "finished": true, "packaging": [{"sample": false, "description": "15 TABLET, FILM COATED in 1 BLISTER PACK (0615-8084-05)", "package_ndc": "0615-8084-05", "marketing_start_date": "20160722"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8084-39)", "package_ndc": "0615-8084-39", "marketing_start_date": "20160722"}], "brand_name": "Cyclobenzaprine Hydrochloride", "product_id": "0615-8084_3af92905-fa00-41fa-9156-037f58b21a0b", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "0615-8084", "generic_name": "Cyclobenzaprine", "labeler_name": "NCS HealthCare of KY, LLC dba Vangard Labs", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cyclobenzaprine Hydrochloride", "active_ingredients": [{"name": "CYCLOBENZAPRINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA090478", "marketing_category": "ANDA", "marketing_start_date": "20160722", "listing_expiration_date": "20261231"}