cyclobenzaprine hydrochloride
Generic: cyclobenzaprine hydrochloride
Labeler: bryant ranch prepackDrug Facts
Product Profile
Brand Name
cyclobenzaprine hydrochloride
Generic Name
cyclobenzaprine hydrochloride
Labeler
bryant ranch prepack
Dosage Form
TABLET
Routes
Active Ingredients
cyclobenzaprine hydrochloride 10 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
71335-2666
Product ID
71335-2666_71c2dd8a-818a-444b-bdfb-9f8b6bc55f3a
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA218936
Listing Expiration
2026-12-31
Marketing Start
2025-02-19
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
713352666
Hyphenated Format
71335-2666
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
ANDA218936 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/1
Packaging
- 40 TABLET in 1 BOTTLE (71335-2666-0)
- 14 TABLET in 1 BOTTLE (71335-2666-1)
- 84 TABLET in 1 BOTTLE (71335-2666-2)
- 30 TABLET in 1 BOTTLE (71335-2666-3)
- 20 TABLET in 1 BOTTLE (71335-2666-4)
- 15 TABLET in 1 BOTTLE (71335-2666-5)
- 60 TABLET in 1 BOTTLE (71335-2666-6)
- 90 TABLET in 1 BOTTLE (71335-2666-7)
- 56 TABLET in 1 BOTTLE (71335-2666-8)
- 120 TABLET in 1 BOTTLE (71335-2666-9)
Packages (10)
71335-2666-0
40 TABLET in 1 BOTTLE (71335-2666-0)
71335-2666-1
14 TABLET in 1 BOTTLE (71335-2666-1)
71335-2666-2
84 TABLET in 1 BOTTLE (71335-2666-2)
71335-2666-3
30 TABLET in 1 BOTTLE (71335-2666-3)
71335-2666-4
20 TABLET in 1 BOTTLE (71335-2666-4)
71335-2666-5
15 TABLET in 1 BOTTLE (71335-2666-5)
71335-2666-6
60 TABLET in 1 BOTTLE (71335-2666-6)
71335-2666-7
90 TABLET in 1 BOTTLE (71335-2666-7)
71335-2666-8
56 TABLET in 1 BOTTLE (71335-2666-8)
71335-2666-9
120 TABLET in 1 BOTTLE (71335-2666-9)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "71c2dd8a-818a-444b-bdfb-9f8b6bc55f3a", "openfda": {"unii": ["0VE05JYS2P"], "rxcui": ["828348"], "spl_set_id": ["6536b470-9a4e-4174-85b8-479f64cc3296"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "40 TABLET in 1 BOTTLE (71335-2666-0)", "package_ndc": "71335-2666-0", "marketing_start_date": "20250714"}, {"sample": false, "description": "14 TABLET in 1 BOTTLE (71335-2666-1)", "package_ndc": "71335-2666-1", "marketing_start_date": "20250714"}, {"sample": false, "description": "84 TABLET in 1 BOTTLE (71335-2666-2)", "package_ndc": "71335-2666-2", "marketing_start_date": "20250714"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-2666-3)", "package_ndc": "71335-2666-3", "marketing_start_date": "20250714"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE (71335-2666-4)", "package_ndc": "71335-2666-4", "marketing_start_date": "20250714"}, {"sample": false, "description": "15 TABLET in 1 BOTTLE (71335-2666-5)", "package_ndc": "71335-2666-5", "marketing_start_date": "20250714"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71335-2666-6)", "package_ndc": "71335-2666-6", "marketing_start_date": "20250714"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-2666-7)", "package_ndc": "71335-2666-7", "marketing_start_date": "20250714"}, {"sample": false, "description": "56 TABLET in 1 BOTTLE (71335-2666-8)", "package_ndc": "71335-2666-8", "marketing_start_date": "20250714"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE (71335-2666-9)", "package_ndc": "71335-2666-9", "marketing_start_date": "20250714"}], "brand_name": "Cyclobenzaprine Hydrochloride", "product_id": "71335-2666_71c2dd8a-818a-444b-bdfb-9f8b6bc55f3a", "dosage_form": "TABLET", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "71335-2666", "generic_name": "Cyclobenzaprine Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cyclobenzaprine Hydrochloride", "active_ingredients": [{"name": "CYCLOBENZAPRINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA218936", "marketing_category": "ANDA", "marketing_start_date": "20250219", "listing_expiration_date": "20261231"}