cyclobenzaprine hydrochloride
Generic: cyclobenzaprine hydrochloride
Labeler: a-s medication solutionsDrug Facts
Product Profile
Brand Name
cyclobenzaprine hydrochloride
Generic Name
cyclobenzaprine hydrochloride
Labeler
a-s medication solutions
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
cyclobenzaprine hydrochloride 10 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
50090-4727
Product ID
50090-4727_0d2d2af6-37df-43fe-8222-c1374734d48a
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA208170
Listing Expiration
2026-12-31
Marketing Start
2017-05-31
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
500904727
Hyphenated Format
50090-4727
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 hydrochloride (source: ndc)
Application Number
ANDA208170 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/1
Packaging
- 15 TABLET, FILM COATED in 1 BOTTLE (50090-4727-0)
- 20 TABLET, FILM COATED in 1 BOTTLE (50090-4727-1)
- 30 TABLET, FILM COATED in 1 BOTTLE (50090-4727-2)
- 60 TABLET, FILM COATED in 1 BOTTLE (50090-4727-3)
- 100 TABLET, FILM COATED in 1 BOTTLE (50090-4727-4)
- 7 TABLET, FILM COATED in 1 BOTTLE (50090-4727-6)
- 14 TABLET, FILM COATED in 1 BOTTLE (50090-4727-7)
- 21 TABLET, FILM COATED in 1 BOTTLE (50090-4727-8)
- 10 TABLET, FILM COATED in 1 BOTTLE (50090-4727-9)
Packages (9)
50090-4727-0
15 TABLET, FILM COATED in 1 BOTTLE (50090-4727-0)
50090-4727-1
20 TABLET, FILM COATED in 1 BOTTLE (50090-4727-1)
50090-4727-2
30 TABLET, FILM COATED in 1 BOTTLE (50090-4727-2)
50090-4727-3
60 TABLET, FILM COATED in 1 BOTTLE (50090-4727-3)
50090-4727-4
100 TABLET, FILM COATED in 1 BOTTLE (50090-4727-4)
50090-4727-6
7 TABLET, FILM COATED in 1 BOTTLE (50090-4727-6)
50090-4727-7
14 TABLET, FILM COATED in 1 BOTTLE (50090-4727-7)
50090-4727-8
21 TABLET, FILM COATED in 1 BOTTLE (50090-4727-8)
50090-4727-9
10 TABLET, FILM COATED in 1 BOTTLE (50090-4727-9)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0d2d2af6-37df-43fe-8222-c1374734d48a", "openfda": {"unii": ["0VE05JYS2P"], "rxcui": ["828348"], "spl_set_id": ["eb908b77-741c-473a-b2e9-4f82167c3088"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "15 TABLET, FILM COATED in 1 BOTTLE (50090-4727-0)", "package_ndc": "50090-4727-0", "marketing_start_date": "20191118"}, {"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (50090-4727-1)", "package_ndc": "50090-4727-1", "marketing_start_date": "20191118"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (50090-4727-2)", "package_ndc": "50090-4727-2", "marketing_start_date": "20191118"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (50090-4727-3)", "package_ndc": "50090-4727-3", "marketing_start_date": "20191118"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (50090-4727-4)", "package_ndc": "50090-4727-4", "marketing_start_date": "20191118"}, {"sample": false, "description": "7 TABLET, FILM COATED in 1 BOTTLE (50090-4727-6)", "package_ndc": "50090-4727-6", "marketing_start_date": "20191118"}, {"sample": false, "description": "14 TABLET, FILM COATED in 1 BOTTLE (50090-4727-7)", "package_ndc": "50090-4727-7", "marketing_start_date": "20191118"}, {"sample": false, "description": "21 TABLET, FILM COATED in 1 BOTTLE (50090-4727-8)", "package_ndc": "50090-4727-8", "marketing_start_date": "20191118"}, {"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE (50090-4727-9)", "package_ndc": "50090-4727-9", "marketing_start_date": "20191118"}], "brand_name": "CYCLOBENZAPRINE HYDROCHLORIDE", "product_id": "50090-4727_0d2d2af6-37df-43fe-8222-c1374734d48a", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "50090-4727", "generic_name": "cyclobenzaprine hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CYCLOBENZAPRINE HYDROCHLORIDE", "active_ingredients": [{"name": "CYCLOBENZAPRINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA208170", "marketing_category": "ANDA", "marketing_start_date": "20170531", "listing_expiration_date": "20261231"}