diazepam

Generic: diazepam

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name diazepam
Generic Name diazepam
Labeler proficient rx lp
Dosage Form TABLET
Routes
ORAL
Active Ingredients

diazepam 10 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 82804-186
Product ID 82804-186_9322b0bc-e9fa-4c89-808b-110decf6db58
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA217843
DEA Schedule civ
Listing Expiration 2026-12-31
Marketing Start 2023-12-14

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 82804186
Hyphenated Format 82804-186

Supplemental Identifiers

RxCUI
197589
UPC
0382804186303
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 ANDA217843 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (82804-186-30)
source: ndc

Packages (1)

82804-186-30 30 TABLET in 1 BOTTLE (82804-186-30)

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": "9322b0bc-e9fa-4c89-808b-110decf6db58", "openfda": {"nui": ["N0000175694", "M0002356"], "upc": ["0382804186303"], "unii": ["Q3JTX2Q7TU"], "rxcui": ["197589"], "spl_set_id": ["9322b0bc-e9fa-4c89-808b-110decf6db58"], "pharm_class_cs": ["Benzodiazepines [CS]"], "pharm_class_epc": ["Benzodiazepine [EPC]"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (82804-186-30)", "package_ndc": "82804-186-30", "marketing_start_date": "20250114"}], "brand_name": "DIAZEPAM", "product_id": "82804-186_9322b0bc-e9fa-4c89-808b-110decf6db58", "dosage_form": "TABLET", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "82804-186", "dea_schedule": "CIV", "generic_name": "DIAZEPAM", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DIAZEPAM", "active_ingredients": [{"name": "DIAZEPAM", "strength": "10 mg/1"}], "application_number": "ANDA217843", "marketing_category": "ANDA", "marketing_start_date": "20231214", "listing_expiration_date": "20261231"}