diazepam

Generic: diazepam

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name diazepam
Generic Name diazepam
Labeler bryant ranch prepack
Dosage Form TABLET
Routes
ORAL
Active Ingredients

diazepam 10 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-0444
Product ID 71335-0444_5f5a6893-926b-4934-bdcd-b1c0efedf319
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA071322
DEA Schedule civ
Listing Expiration 2026-12-31
Marketing Start 1986-12-10

Pharmacologic Class

Established (EPC)
benzodiazepine [epc]
Chemical Structure
benzodiazepines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 713350444
Hyphenated Format 71335-0444

Supplemental Identifiers

RxCUI
197589
UNII
Q3JTX2Q7TU
NUI
N0000175694 M0002356

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 ANDA071322 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 56 TABLET in 1 BOTTLE (71335-0444-0)
  • 20 TABLET in 1 BOTTLE (71335-0444-1)
  • 30 TABLET in 1 BOTTLE (71335-0444-2)
  • 40 TABLET in 1 BOTTLE (71335-0444-3)
  • 50 TABLET in 1 BOTTLE (71335-0444-4)
  • 60 TABLET in 1 BOTTLE (71335-0444-5)
  • 90 TABLET in 1 BOTTLE (71335-0444-6)
  • 100 TABLET in 1 BOTTLE (71335-0444-7)
  • 10 TABLET in 1 BOTTLE (71335-0444-8)
  • 120 TABLET in 1 BOTTLE (71335-0444-9)
source: ndc

Packages (10)

71335-0444-0 56 TABLET in 1 BOTTLE (71335-0444-0) 71335-0444-1 20 TABLET in 1 BOTTLE (71335-0444-1) 71335-0444-2 30 TABLET in 1 BOTTLE (71335-0444-2) 71335-0444-3 40 TABLET in 1 BOTTLE (71335-0444-3) 71335-0444-4 50 TABLET in 1 BOTTLE (71335-0444-4) 71335-0444-5 60 TABLET in 1 BOTTLE (71335-0444-5) 71335-0444-6 90 TABLET in 1 BOTTLE (71335-0444-6) 71335-0444-7 100 TABLET in 1 BOTTLE (71335-0444-7) 71335-0444-8 10 TABLET in 1 BOTTLE (71335-0444-8) 71335-0444-9 120 TABLET in 1 BOTTLE (71335-0444-9)

Ingredients (1)

diazepam (10 mg/1)

Linked Drug Pages (1)

Diazepam ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "5f5a6893-926b-4934-bdcd-b1c0efedf319", "openfda": {"nui": ["N0000175694", "M0002356"], "unii": ["Q3JTX2Q7TU"], "rxcui": ["197589"], "spl_set_id": ["078bbb41-7e3a-48db-87f0-ec6a6ec0194e"], "pharm_class_cs": ["Benzodiazepines [CS]"], "pharm_class_epc": ["Benzodiazepine [EPC]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "56 TABLET in 1 BOTTLE (71335-0444-0)", "package_ndc": "71335-0444-0", "marketing_start_date": "20240403"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE (71335-0444-1)", "package_ndc": "71335-0444-1", "marketing_start_date": "20190726"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-0444-2)", "package_ndc": "71335-0444-2", "marketing_start_date": "20180214"}, {"sample": false, "description": "40 TABLET in 1 BOTTLE (71335-0444-3)", "package_ndc": "71335-0444-3", "marketing_start_date": "20180227"}, {"sample": false, "description": "50 TABLET in 1 BOTTLE (71335-0444-4)", "package_ndc": "71335-0444-4", "marketing_start_date": "20240403"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71335-0444-5)", "package_ndc": "71335-0444-5", "marketing_start_date": "20180219"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-0444-6)", "package_ndc": "71335-0444-6", "marketing_start_date": "20180306"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (71335-0444-7)", "package_ndc": "71335-0444-7", "marketing_start_date": "20240403"}, {"sample": false, "description": "10 TABLET in 1 BOTTLE (71335-0444-8)", "package_ndc": "71335-0444-8", "marketing_start_date": "20190325"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE (71335-0444-9)", "package_ndc": "71335-0444-9", "marketing_start_date": "20180723"}], "brand_name": "Diazepam", "product_id": "71335-0444_5f5a6893-926b-4934-bdcd-b1c0efedf319", "dosage_form": "TABLET", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "71335-0444", "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": "10 mg/1"}], "application_number": "ANDA071322", "marketing_category": "ANDA", "marketing_start_date": "19861210", "listing_expiration_date": "20261231"}