cyclobenzaprine hydrochloride
Generic: cyclobenzaprine hydrochloride
Labeler: asclemed usa, inc.Drug Facts
Product Profile
Brand Name
cyclobenzaprine hydrochloride
Generic Name
cyclobenzaprine hydrochloride
Labeler
asclemed usa, inc.
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
cyclobenzaprine hydrochloride 7.5 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
76420-840
Product ID
76420-840_3b4cbe13-2679-7313-e063-6294a90a97ae
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA213324
Listing Expiration
2026-12-31
Marketing Start
2020-07-06
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
76420840
Hyphenated Format
76420-840
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
ANDA213324 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 7.5 mg/1
Packaging
- 1000 TABLET, FILM COATED in 1 BOTTLE (76420-840-00)
- 1 TABLET, FILM COATED in 1 BOTTLE (76420-840-01)
- 2 TABLET, FILM COATED in 1 BOTTLE (76420-840-02)
- 7 TABLET, FILM COATED in 1 BOTTLE (76420-840-07)
- 100 TABLET, FILM COATED in 1 BOTTLE (76420-840-10)
- 20 TABLET, FILM COATED in 1 BOTTLE (76420-840-20)
- 30 TABLET, FILM COATED in 1 BOTTLE (76420-840-30)
- 60 TABLET, FILM COATED in 1 BOTTLE (76420-840-60)
- 90 TABLET, FILM COATED in 1 BOTTLE (76420-840-90)
Packages (9)
76420-840-00
1000 TABLET, FILM COATED in 1 BOTTLE (76420-840-00)
76420-840-01
1 TABLET, FILM COATED in 1 BOTTLE (76420-840-01)
76420-840-02
2 TABLET, FILM COATED in 1 BOTTLE (76420-840-02)
76420-840-07
7 TABLET, FILM COATED in 1 BOTTLE (76420-840-07)
76420-840-10
100 TABLET, FILM COATED in 1 BOTTLE (76420-840-10)
76420-840-20
20 TABLET, FILM COATED in 1 BOTTLE (76420-840-20)
76420-840-30
30 TABLET, FILM COATED in 1 BOTTLE (76420-840-30)
76420-840-60
60 TABLET, FILM COATED in 1 BOTTLE (76420-840-60)
76420-840-90
90 TABLET, FILM COATED in 1 BOTTLE (76420-840-90)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3b4cbe13-2679-7313-e063-6294a90a97ae", "openfda": {"unii": ["0VE05JYS2P"], "rxcui": ["828299", "828320", "828348"], "spl_set_id": ["820dca15-5b7f-41e0-955f-73f942709264"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (76420-840-00)", "package_ndc": "76420-840-00", "marketing_start_date": "20240816"}, {"sample": false, "description": "1 TABLET, FILM COATED in 1 BOTTLE (76420-840-01)", "package_ndc": "76420-840-01", "marketing_start_date": "20240816"}, {"sample": false, "description": "2 TABLET, FILM COATED in 1 BOTTLE (76420-840-02)", "package_ndc": "76420-840-02", "marketing_start_date": "20240816"}, {"sample": false, "description": "7 TABLET, FILM COATED in 1 BOTTLE (76420-840-07)", "package_ndc": "76420-840-07", "marketing_start_date": "20240816"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (76420-840-10)", "package_ndc": "76420-840-10", "marketing_start_date": "20240816"}, {"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (76420-840-20)", "package_ndc": "76420-840-20", "marketing_start_date": "20240816"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (76420-840-30)", "package_ndc": "76420-840-30", "marketing_start_date": "20240816"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (76420-840-60)", "package_ndc": "76420-840-60", "marketing_start_date": "20240816"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (76420-840-90)", "package_ndc": "76420-840-90", "marketing_start_date": "20240816"}], "brand_name": "Cyclobenzaprine hydrochloride", "product_id": "76420-840_3b4cbe13-2679-7313-e063-6294a90a97ae", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "76420-840", "generic_name": "Cyclobenzaprine hydrochloride", "labeler_name": "Asclemed USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cyclobenzaprine hydrochloride", "active_ingredients": [{"name": "CYCLOBENZAPRINE HYDROCHLORIDE", "strength": "7.5 mg/1"}], "application_number": "ANDA213324", "marketing_category": "ANDA", "marketing_start_date": "20200706", "listing_expiration_date": "20261231"}