cyclobenzaprine hydrochloride
Generic: cyclobenzaprine hydrochloride
Labeler: avkareDrug Facts
Product Profile
Brand Name
cyclobenzaprine hydrochloride
Generic Name
cyclobenzaprine hydrochloride
Labeler
avkare
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
cyclobenzaprine hydrochloride 10 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
42291-154
Product ID
42291-154_3ab20dcb-627a-53c4-e063-6394a90a20cb
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA077563
Listing Expiration
2026-12-31
Marketing Start
2020-04-03
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
42291154
Hyphenated Format
42291-154
Supplemental Identifiers
RxCUI
UPC
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 hydrochloride (source: ndc)
Application Number
ANDA077563 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/1
Packaging
- 1000 TABLET, FILM COATED in 1 BOTTLE (42291-154-10)
- 120 TABLET, FILM COATED in 1 BOTTLE (42291-154-12)
- 180 TABLET, FILM COATED in 1 BOTTLE (42291-154-18)
- 270 TABLET, FILM COATED in 1 BOTTLE (42291-154-27)
- 30 TABLET, FILM COATED in 1 BOTTLE (42291-154-30)
- 45 TABLET, FILM COATED in 1 BOTTLE (42291-154-45)
- 60 TABLET, FILM COATED in 1 BOTTLE (42291-154-60)
- 90 TABLET, FILM COATED in 1 BOTTLE (42291-154-90)
Packages (8)
42291-154-10
1000 TABLET, FILM COATED in 1 BOTTLE (42291-154-10)
42291-154-12
120 TABLET, FILM COATED in 1 BOTTLE (42291-154-12)
42291-154-18
180 TABLET, FILM COATED in 1 BOTTLE (42291-154-18)
42291-154-27
270 TABLET, FILM COATED in 1 BOTTLE (42291-154-27)
42291-154-30
30 TABLET, FILM COATED in 1 BOTTLE (42291-154-30)
42291-154-45
45 TABLET, FILM COATED in 1 BOTTLE (42291-154-45)
42291-154-60
60 TABLET, FILM COATED in 1 BOTTLE (42291-154-60)
42291-154-90
90 TABLET, FILM COATED in 1 BOTTLE (42291-154-90)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3ab20dcb-627a-53c4-e063-6394a90a20cb", "openfda": {"upc": ["0342291154605"], "unii": ["0VE05JYS2P"], "rxcui": ["828348"], "spl_set_id": ["a264ab9f-cc12-325f-e053-2a95a90a53d9"], "manufacturer_name": ["AvKARE"]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (42291-154-10)", "package_ndc": "42291-154-10", "marketing_start_date": "20200403"}, {"sample": false, "description": "120 TABLET, FILM COATED in 1 BOTTLE (42291-154-12)", "package_ndc": "42291-154-12", "marketing_start_date": "20200403"}, {"sample": false, "description": "180 TABLET, FILM COATED in 1 BOTTLE (42291-154-18)", "package_ndc": "42291-154-18", "marketing_start_date": "20200403"}, {"sample": false, "description": "270 TABLET, FILM COATED in 1 BOTTLE (42291-154-27)", "package_ndc": "42291-154-27", "marketing_start_date": "20200403"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (42291-154-30)", "package_ndc": "42291-154-30", "marketing_start_date": "20200403"}, {"sample": false, "description": "45 TABLET, FILM COATED in 1 BOTTLE (42291-154-45)", "package_ndc": "42291-154-45", "marketing_start_date": "20200403"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (42291-154-60)", "package_ndc": "42291-154-60", "marketing_start_date": "20200403"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (42291-154-90)", "package_ndc": "42291-154-90", "marketing_start_date": "20200403"}], "brand_name": "Cyclobenzaprine Hydrochloride", "product_id": "42291-154_3ab20dcb-627a-53c4-e063-6394a90a20cb", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "42291-154", "generic_name": "Cyclobenzaprine Hydrochloride", "labeler_name": "AvKARE", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cyclobenzaprine Hydrochloride", "active_ingredients": [{"name": "CYCLOBENZAPRINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA077563", "marketing_category": "ANDA", "marketing_start_date": "20200403", "listing_expiration_date": "20261231"}