cyclobenzaprine hydrochloride

Generic: cyclobenzaprine hydrochloride

Labeler: redpharm drug
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name cyclobenzaprine hydrochloride
Generic Name cyclobenzaprine hydrochloride
Labeler redpharm drug
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

cyclobenzaprine hydrochloride 10 mg/1

Manufacturer
Redpharm Drug

Identifiers & Regulatory

Product NDC 67296-2084
Product ID 67296-2084_325396d0-0b56-4858-e063-6294a90a29e1
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA208170
Listing Expiration 2026-12-31
Marketing Start 2017-05-31

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 672962084
Hyphenated Format 67296-2084

Supplemental Identifiers

RxCUI
828348
UPC
0372888012001 0372888012018 0372888012056 0372888014005 0372888014050 0372888013015 0372888014012
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 ANDA208170 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 15 TABLET, FILM COATED in 1 BOTTLE (67296-2084-1)
  • 10 TABLET, FILM COATED in 1 BOTTLE (67296-2084-2)
  • 30 TABLET, FILM COATED in 1 BOTTLE (67296-2084-3)
  • 21 TABLET, FILM COATED in 1 BOTTLE (67296-2084-4)
source: ndc

Packages (4)

67296-2084-1 15 TABLET, FILM COATED in 1 BOTTLE (67296-2084-1) 67296-2084-2 10 TABLET, FILM COATED in 1 BOTTLE (67296-2084-2) 67296-2084-3 30 TABLET, FILM COATED in 1 BOTTLE (67296-2084-3) 67296-2084-4 21 TABLET, FILM COATED in 1 BOTTLE (67296-2084-4)

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": "325396d0-0b56-4858-e063-6294a90a29e1", "openfda": {"upc": ["0372888012001", "0372888012018", "0372888012056", "0372888014005", "0372888014050", "0372888013015", "0372888014012"], "unii": ["0VE05JYS2P"], "rxcui": ["828348"], "spl_set_id": ["0ab1b6f8-5d73-f97a-e063-6294a90a9fbf"], "manufacturer_name": ["Redpharm Drug"]}, "finished": true, "packaging": [{"sample": false, "description": "15 TABLET, FILM COATED in 1 BOTTLE (67296-2084-1)", "package_ndc": "67296-2084-1", "marketing_start_date": "20170531"}, {"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE (67296-2084-2)", "package_ndc": "67296-2084-2", "marketing_start_date": "20170531"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (67296-2084-3)", "package_ndc": "67296-2084-3", "marketing_start_date": "20170531"}, {"sample": false, "description": "21 TABLET, FILM COATED in 1 BOTTLE (67296-2084-4)", "package_ndc": "67296-2084-4", "marketing_start_date": "20170531"}], "brand_name": "CYCLOBENZAPRINE HYDROCHLORIDE", "product_id": "67296-2084_325396d0-0b56-4858-e063-6294a90a29e1", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "67296-2084", "generic_name": "cyclobenzaprine hydrochloride", "labeler_name": "Redpharm Drug", "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"}