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 67296-1893
Product ID 67296-1893_2c631fa5-2dbd-5a58-e063-6394a90ab1e2
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078643
Listing Expiration 2026-12-31
Marketing Start 2008-09-26

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 672961893
Hyphenated Format 67296-1893

Supplemental Identifiers

RxCUI
828348
UPC
0316571782017 0316571783014
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 ANDA078643 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 10 TABLET, FILM COATED in 1 BOTTLE (67296-1893-1)
  • 15 TABLET, FILM COATED in 1 BOTTLE (67296-1893-7)
source: ndc

Packages (2)

67296-1893-1 10 TABLET, FILM COATED in 1 BOTTLE (67296-1893-1) 67296-1893-7 15 TABLET, FILM COATED in 1 BOTTLE (67296-1893-7)

Ingredients (1)

cyclobenzaprine hydrochloride (10 mg/1)

Linked Drug Pages (2)

Cyclobenzaprine Hydrochloride ndc-match (0.9) Cyclobenzaprine Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2c631fa5-2dbd-5a58-e063-6394a90ab1e2", "openfda": {"upc": ["0316571782017", "0316571783014"], "unii": ["0VE05JYS2P"], "rxcui": ["828348"], "spl_set_id": ["fc61c9f5-b0ec-3ff8-e053-6394a90adeb7"], "manufacturer_name": ["Redpharm Drug"]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE (67296-1893-1)", "package_ndc": "67296-1893-1", "marketing_start_date": "20080926"}, {"sample": false, "description": "15 TABLET, FILM COATED in 1 BOTTLE (67296-1893-7)", "package_ndc": "67296-1893-7", "marketing_start_date": "20080926"}], "brand_name": "Cyclobenzaprine Hydrochloride", "product_id": "67296-1893_2c631fa5-2dbd-5a58-e063-6394a90ab1e2", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "67296-1893", "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": "ANDA078643", "marketing_category": "ANDA", "marketing_start_date": "20080926", "listing_expiration_date": "20261231"}