diazepam
Generic: diazepam
Labeler: bryant ranch prepackDrug Facts
Product Profile
Brand Name
diazepam
Generic Name
diazepam
Labeler
bryant ranch prepack
Dosage Form
TABLET
Routes
Active Ingredients
diazepam 5 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
71335-1584
Product ID
71335-1584_dc33c03b-c55f-4b37-9b2b-85c949d2a1c3
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA071321
DEA Schedule
civ
Listing Expiration
2026-12-31
Marketing Start
1986-12-10
Pharmacologic Class
Established (EPC)
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
713351584
Hyphenated Format
71335-1584
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
diazepam (source: ndc)
Generic Name
diazepam (source: ndc)
Application Number
ANDA071321 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 5 mg/1
Packaging
- 120 TABLET in 1 BOTTLE (71335-1584-0)
- 12 TABLET in 1 BOTTLE (71335-1584-1)
- 15 TABLET in 1 BOTTLE (71335-1584-2)
- 20 TABLET in 1 BOTTLE (71335-1584-3)
- 30 TABLET in 1 BOTTLE (71335-1584-4)
- 60 TABLET in 1 BOTTLE (71335-1584-5)
- 90 TABLET in 1 BOTTLE (71335-1584-6)
- 10 TABLET in 1 BOTTLE (71335-1584-7)
- 2 TABLET in 1 BOTTLE (71335-1584-8)
- 1 TABLET in 1 BOTTLE (71335-1584-9)
Packages (10)
71335-1584-0
120 TABLET in 1 BOTTLE (71335-1584-0)
71335-1584-1
12 TABLET in 1 BOTTLE (71335-1584-1)
71335-1584-2
15 TABLET in 1 BOTTLE (71335-1584-2)
71335-1584-3
20 TABLET in 1 BOTTLE (71335-1584-3)
71335-1584-4
30 TABLET in 1 BOTTLE (71335-1584-4)
71335-1584-5
60 TABLET in 1 BOTTLE (71335-1584-5)
71335-1584-6
90 TABLET in 1 BOTTLE (71335-1584-6)
71335-1584-7
10 TABLET in 1 BOTTLE (71335-1584-7)
71335-1584-8
2 TABLET in 1 BOTTLE (71335-1584-8)
71335-1584-9
1 TABLET in 1 BOTTLE (71335-1584-9)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "dc33c03b-c55f-4b37-9b2b-85c949d2a1c3", "openfda": {"nui": ["N0000175694", "M0002356"], "unii": ["Q3JTX2Q7TU"], "rxcui": ["197591"], "spl_set_id": ["6abedac6-5133-47b2-a0e3-e239e0a2254b"], "pharm_class_cs": ["Benzodiazepines [CS]"], "pharm_class_epc": ["Benzodiazepine [EPC]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "120 TABLET in 1 BOTTLE (71335-1584-0)", "package_ndc": "71335-1584-0", "marketing_start_date": "20220210"}, {"sample": false, "description": "12 TABLET in 1 BOTTLE (71335-1584-1)", "package_ndc": "71335-1584-1", "marketing_start_date": "20220210"}, {"sample": false, "description": "15 TABLET in 1 BOTTLE (71335-1584-2)", "package_ndc": "71335-1584-2", "marketing_start_date": "20220210"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE (71335-1584-3)", "package_ndc": "71335-1584-3", "marketing_start_date": "20220210"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-1584-4)", "package_ndc": "71335-1584-4", "marketing_start_date": "20220210"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71335-1584-5)", "package_ndc": "71335-1584-5", "marketing_start_date": "20220210"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-1584-6)", "package_ndc": "71335-1584-6", "marketing_start_date": "20220210"}, {"sample": false, "description": "10 TABLET in 1 BOTTLE (71335-1584-7)", "package_ndc": "71335-1584-7", "marketing_start_date": "20220210"}, {"sample": false, "description": "2 TABLET in 1 BOTTLE (71335-1584-8)", "package_ndc": "71335-1584-8", "marketing_start_date": "20220210"}, {"sample": false, "description": "1 TABLET in 1 BOTTLE (71335-1584-9)", "package_ndc": "71335-1584-9", "marketing_start_date": "20220210"}], "brand_name": "Diazepam", "product_id": "71335-1584_dc33c03b-c55f-4b37-9b2b-85c949d2a1c3", "dosage_form": "TABLET", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "71335-1584", "dea_schedule": "CIV", "generic_name": "Diazepam", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diazepam", "active_ingredients": [{"name": "DIAZEPAM", "strength": "5 mg/1"}], "application_number": "ANDA071321", "marketing_category": "ANDA", "marketing_start_date": "19861210", "listing_expiration_date": "20261231"}