diazepam

Generic: diazepam

Labeler: direct_rx
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name diazepam
Generic Name diazepam
Labeler direct_rx
Dosage Form TABLET
Routes
ORAL
Active Ingredients

diazepam 10 mg/1

Manufacturer
Direct_Rx

Identifiers & Regulatory

Product NDC 61919-906
Product ID 61919-906_47e14ab4-5eb5-67c7-e063-6394a90a1e4b
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA071322
DEA Schedule civ
Listing Expiration 2027-12-31
Marketing Start 2016-11-01

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 61919906
Hyphenated Format 61919-906

Supplemental Identifiers

RxCUI
197589 197591
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
  • 2 TABLET in 1 BOTTLE (61919-906-02)
  • 5 TABLET in 1 BOTTLE (61919-906-05)
  • 10 TABLET in 1 BOTTLE (61919-906-10)
  • 30 TABLET in 1 BOTTLE (61919-906-30)
  • 60 TABLET in 1 BOTTLE (61919-906-60)
  • 90 TABLET in 1 BOTTLE (61919-906-90)
source: ndc

Packages (6)

61919-906-02 2 TABLET in 1 BOTTLE (61919-906-02) 61919-906-05 5 TABLET in 1 BOTTLE (61919-906-05) 61919-906-10 10 TABLET in 1 BOTTLE (61919-906-10) 61919-906-30 30 TABLET in 1 BOTTLE (61919-906-30) 61919-906-60 60 TABLET in 1 BOTTLE (61919-906-60) 61919-906-90 90 TABLET in 1 BOTTLE (61919-906-90)

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": "47e14ab4-5eb5-67c7-e063-6394a90a1e4b", "openfda": {"nui": ["N0000175694", "M0002356"], "unii": ["Q3JTX2Q7TU"], "rxcui": ["197589", "197591"], "spl_set_id": ["4b0c9c0a-4274-4d56-a7a4-bc497916469c"], "pharm_class_cs": ["Benzodiazepines [CS]"], "pharm_class_epc": ["Benzodiazepine [EPC]"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "2 TABLET in 1 BOTTLE (61919-906-02)", "package_ndc": "61919-906-02", "marketing_start_date": "20161101"}, {"sample": false, "description": "5 TABLET in 1 BOTTLE (61919-906-05)", "package_ndc": "61919-906-05", "marketing_start_date": "20190925"}, {"sample": false, "description": "10 TABLET in 1 BOTTLE (61919-906-10)", "package_ndc": "61919-906-10", "marketing_start_date": "20161101"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (61919-906-30)", "package_ndc": "61919-906-30", "marketing_start_date": "20161101"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (61919-906-60)", "package_ndc": "61919-906-60", "marketing_start_date": "20161101"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (61919-906-90)", "package_ndc": "61919-906-90", "marketing_start_date": "20161101"}], "brand_name": "DIAZEPAM", "product_id": "61919-906_47e14ab4-5eb5-67c7-e063-6394a90a1e4b", "dosage_form": "TABLET", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "61919-906", "dea_schedule": "CIV", "generic_name": "DIAZEPAM", "labeler_name": "Direct_Rx", "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": "20161101", "listing_expiration_date": "20271231"}