Cyclobenzaprine hydrochloride

Generic: Cyclobenzaprine hydrochloride

Labeler: Quality Care Products, LLC
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive

Drug Facts

Product Profile

Brand Name Cyclobenzaprine hydrochloride
Generic Name Cyclobenzaprine hydrochloride
Labeler Quality Care Products, LLC
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1

Identifiers & Regulatory

Product NDC 55700-925
Product ID 55700-925_bcc88669-9da7-4a66-8add-b6f439c0b52e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA213324
Marketing Start 2021-10-05
Marketing End 2026-02-28

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 55700925
Hyphenated Format 55700-925

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 ANDA213324 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (55700-925-30)
  • 60 TABLET, FILM COATED in 1 BOTTLE (55700-925-60)
  • 90 TABLET, FILM COATED in 1 BOTTLE (55700-925-90)
source: ndc

Packages (3)

55700-925-30 30 TABLET, FILM COATED in 1 BOTTLE (55700-925-30) 55700-925-60 60 TABLET, FILM COATED in 1 BOTTLE (55700-925-60) 55700-925-90 90 TABLET, FILM COATED in 1 BOTTLE (55700-925-90)

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": "bcc88669-9da7-4a66-8add-b6f439c0b52e", "openfda": {"unii": ["0VE05JYS2P"], "rxcui": ["828320", "828348"], "spl_set_id": ["19a54d55-a79a-48c0-89d0-dedd0dcf9f45"], "manufacturer_name": ["Quality Care Products, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (55700-925-30)", "package_ndc": "55700-925-30", "marketing_end_date": "20260228", "marketing_start_date": "20211005"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (55700-925-60)", "package_ndc": "55700-925-60", "marketing_end_date": "20260228", "marketing_start_date": "20211005"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (55700-925-90)", "package_ndc": "55700-925-90", "marketing_end_date": "20260228", "marketing_start_date": "20211005"}], "brand_name": "Cyclobenzaprine hydrochloride", "product_id": "55700-925_bcc88669-9da7-4a66-8add-b6f439c0b52e", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "55700-925", "generic_name": "Cyclobenzaprine hydrochloride", "labeler_name": "Quality Care Products, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cyclobenzaprine hydrochloride", "active_ingredients": [{"name": "CYCLOBENZAPRINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA213324", "marketing_category": "ANDA", "marketing_end_date": "20260228", "marketing_start_date": "20211005"}