cyclobenzaprine hydrochloride

Generic: cyclobenzaprine hydrochloride

Labeler: aphena pharma solutions - tennessee, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name cyclobenzaprine hydrochloride
Generic Name cyclobenzaprine hydrochloride
Labeler aphena pharma solutions - tennessee, llc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

cyclobenzaprine hydrochloride 10 mg/1

Manufacturer
Aphena Pharma Solutions - Tennessee, LLC

Identifiers & Regulatory

Product NDC 71610-907
Product ID 71610-907_37b2aadd-c544-9ecf-e063-6394a90a2cb0
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077563
Listing Expiration 2026-12-31
Marketing Start 2020-04-03

Pharmacologic Class

Classes
centrally-mediated muscle relaxation [pe] muscle relaxant [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 71610907
Hyphenated Format 71610-907

Supplemental Identifiers

RxCUI
828348
UNII
0VE05JYS2P

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
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 45 TABLET, FILM COATED in 1 BOTTLE (71610-907-45)
  • 60 TABLET, FILM COATED in 1 BOTTLE (71610-907-53)
source: ndc

Packages (2)

71610-907-45 45 TABLET, FILM COATED in 1 BOTTLE (71610-907-45) 71610-907-53 60 TABLET, FILM COATED in 1 BOTTLE (71610-907-53)

Ingredients (1)

cyclobenzaprine hydrochloride (10 mg/1)

Linked Drug Pages (1)

Cyclobenzaprine Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "37b2aadd-c544-9ecf-e063-6394a90a2cb0", "openfda": {"unii": ["0VE05JYS2P"], "rxcui": ["828348"], "spl_set_id": ["34f4e63a-1259-0226-e063-6294a90a9fc4"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "45 TABLET, FILM COATED in 1 BOTTLE (71610-907-45)", "package_ndc": "71610-907-45", "marketing_start_date": "20250508"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71610-907-53)", "package_ndc": "71610-907-53", "marketing_start_date": "20250613"}], "brand_name": "Cyclobenzaprine Hydrochloride", "product_id": "71610-907_37b2aadd-c544-9ecf-e063-6394a90a2cb0", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "71610-907", "generic_name": "Cyclobenzaprine Hydrochloride", "labeler_name": "Aphena Pharma Solutions - Tennessee, LLC", "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"}