clonazepam
Generic: clonazepam
Labeler: bryant ranch prepackDrug Facts
Product Profile
Brand Name
clonazepam
Generic Name
clonazepam
Labeler
bryant ranch prepack
Dosage Form
TABLET
Routes
Active Ingredients
clonazepam 1 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
71335-0022
Product ID
71335-0022_4d7caa37-bb59-488b-91c8-db7a6d5a7f87
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA077147
DEA Schedule
civ
Listing Expiration
2026-12-31
Marketing Start
2011-06-03
Pharmacologic Class
Established (EPC)
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
713350022
Hyphenated Format
71335-0022
Supplemental Identifiers
RxCUI
UNII
NUI
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
clonazepam (source: ndc)
Generic Name
clonazepam (source: ndc)
Application Number
ANDA077147 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1 mg/1
Packaging
- 100 TABLET in 1 BOTTLE (71335-0022-0)
- 20 TABLET in 1 BOTTLE (71335-0022-1)
- 30 TABLET in 1 BOTTLE (71335-0022-2)
- 60 TABLET in 1 BOTTLE (71335-0022-3)
- 90 TABLET in 1 BOTTLE (71335-0022-4)
- 120 TABLET in 1 BOTTLE (71335-0022-5)
- 180 TABLET in 1 BOTTLE (71335-0022-6)
- 84 TABLET in 1 BOTTLE (71335-0022-7)
- 28 TABLET in 1 BOTTLE (71335-0022-8)
- 56 TABLET in 1 BOTTLE (71335-0022-9)
Packages (10)
71335-0022-0
100 TABLET in 1 BOTTLE (71335-0022-0)
71335-0022-1
20 TABLET in 1 BOTTLE (71335-0022-1)
71335-0022-2
30 TABLET in 1 BOTTLE (71335-0022-2)
71335-0022-3
60 TABLET in 1 BOTTLE (71335-0022-3)
71335-0022-4
90 TABLET in 1 BOTTLE (71335-0022-4)
71335-0022-5
120 TABLET in 1 BOTTLE (71335-0022-5)
71335-0022-6
180 TABLET in 1 BOTTLE (71335-0022-6)
71335-0022-7
84 TABLET in 1 BOTTLE (71335-0022-7)
71335-0022-8
28 TABLET in 1 BOTTLE (71335-0022-8)
71335-0022-9
56 TABLET in 1 BOTTLE (71335-0022-9)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4d7caa37-bb59-488b-91c8-db7a6d5a7f87", "openfda": {"nui": ["N0000175694", "M0002356"], "unii": ["5PE9FDE8GB"], "rxcui": ["197528"], "spl_set_id": ["4b5240a8-9e87-4664-8698-596a144d6d28"], "pharm_class_cs": ["Benzodiazepines [CS]"], "pharm_class_epc": ["Benzodiazepine [EPC]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (71335-0022-0)", "package_ndc": "71335-0022-0", "marketing_start_date": "20211227"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE (71335-0022-1)", "package_ndc": "71335-0022-1", "marketing_start_date": "20211227"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-0022-2)", "package_ndc": "71335-0022-2", "marketing_start_date": "20180213"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71335-0022-3)", "package_ndc": "71335-0022-3", "marketing_start_date": "20180306"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-0022-4)", "package_ndc": "71335-0022-4", "marketing_start_date": "20180213"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE (71335-0022-5)", "package_ndc": "71335-0022-5", "marketing_start_date": "20180423"}, {"sample": false, "description": "180 TABLET in 1 BOTTLE (71335-0022-6)", "package_ndc": "71335-0022-6", "marketing_start_date": "20211227"}, {"sample": false, "description": "84 TABLET in 1 BOTTLE (71335-0022-7)", "package_ndc": "71335-0022-7", "marketing_start_date": "20180214"}, {"sample": false, "description": "28 TABLET in 1 BOTTLE (71335-0022-8)", "package_ndc": "71335-0022-8", "marketing_start_date": "20180328"}, {"sample": false, "description": "56 TABLET in 1 BOTTLE (71335-0022-9)", "package_ndc": "71335-0022-9", "marketing_start_date": "20180215"}], "brand_name": "Clonazepam", "product_id": "71335-0022_4d7caa37-bb59-488b-91c8-db7a6d5a7f87", "dosage_form": "TABLET", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "71335-0022", "dea_schedule": "CIV", "generic_name": "clonazepam", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Clonazepam", "active_ingredients": [{"name": "CLONAZEPAM", "strength": "1 mg/1"}], "application_number": "ANDA077147", "marketing_category": "ANDA", "marketing_start_date": "20110603", "listing_expiration_date": "20261231"}