diazepam
Generic: diazepam
Labeler: asclemed usa, inc.Drug Facts
Product Profile
Brand Name
diazepam
Generic Name
diazepam
Labeler
asclemed usa, inc.
Dosage Form
TABLET
Routes
Active Ingredients
diazepam 2 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
76420-783
Product ID
76420-783_2cb3e981-e5b2-9d49-e063-6394a90abfbd
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA071307
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
76420783
Hyphenated Format
76420-783
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
ANDA071307 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 2 mg/1
Packaging
- 100 TABLET in 1 BOTTLE (76420-783-01)
- 2 TABLET in 1 BOTTLE (76420-783-02)
- 3 TABLET in 1 BOTTLE (76420-783-03)
- 5 TABLET in 1 BOTTLE (76420-783-05)
- 10 TABLET in 1 BOTTLE (76420-783-10)
- 20 TABLET in 1 BOTTLE (76420-783-20)
- 30 TABLET in 1 BOTTLE (76420-783-30)
- 500 TABLET in 1 BOTTLE (76420-783-55)
- 60 TABLET in 1 BOTTLE (76420-783-60)
- 90 TABLET in 1 BOTTLE (76420-783-90)
Packages (10)
76420-783-01
100 TABLET in 1 BOTTLE (76420-783-01)
76420-783-02
2 TABLET in 1 BOTTLE (76420-783-02)
76420-783-03
3 TABLET in 1 BOTTLE (76420-783-03)
76420-783-05
5 TABLET in 1 BOTTLE (76420-783-05)
76420-783-10
10 TABLET in 1 BOTTLE (76420-783-10)
76420-783-20
20 TABLET in 1 BOTTLE (76420-783-20)
76420-783-30
30 TABLET in 1 BOTTLE (76420-783-30)
76420-783-55
500 TABLET in 1 BOTTLE (76420-783-55)
76420-783-60
60 TABLET in 1 BOTTLE (76420-783-60)
76420-783-90
90 TABLET in 1 BOTTLE (76420-783-90)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2cb3e981-e5b2-9d49-e063-6394a90abfbd", "openfda": {"nui": ["N0000175694", "M0002356"], "unii": ["Q3JTX2Q7TU"], "rxcui": ["197589", "197590", "197591"], "spl_set_id": ["32e7bfa1-6060-4041-a0e5-249cacb84ebc"], "pharm_class_cs": ["Benzodiazepines [CS]"], "pharm_class_epc": ["Benzodiazepine [EPC]"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (76420-783-01)", "package_ndc": "76420-783-01", "marketing_start_date": "20240308"}, {"sample": false, "description": "2 TABLET in 1 BOTTLE (76420-783-02)", "package_ndc": "76420-783-02", "marketing_start_date": "20250127"}, {"sample": false, "description": "3 TABLET in 1 BOTTLE (76420-783-03)", "package_ndc": "76420-783-03", "marketing_start_date": "20250127"}, {"sample": false, "description": "5 TABLET in 1 BOTTLE (76420-783-05)", "package_ndc": "76420-783-05", "marketing_start_date": "20250127"}, {"sample": false, "description": "10 TABLET in 1 BOTTLE (76420-783-10)", "package_ndc": "76420-783-10", "marketing_start_date": "20250127"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE (76420-783-20)", "package_ndc": "76420-783-20", "marketing_start_date": "20250127"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (76420-783-30)", "package_ndc": "76420-783-30", "marketing_start_date": "20240308"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (76420-783-55)", "package_ndc": "76420-783-55", "marketing_start_date": "20250127"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (76420-783-60)", "package_ndc": "76420-783-60", "marketing_start_date": "20240308"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (76420-783-90)", "package_ndc": "76420-783-90", "marketing_start_date": "20240308"}], "brand_name": "Diazepam", "product_id": "76420-783_2cb3e981-e5b2-9d49-e063-6394a90abfbd", "dosage_form": "TABLET", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "76420-783", "dea_schedule": "CIV", "generic_name": "Diazepam", "labeler_name": "Asclemed USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diazepam", "active_ingredients": [{"name": "DIAZEPAM", "strength": "2 mg/1"}], "application_number": "ANDA071307", "marketing_category": "ANDA", "marketing_start_date": "19861210", "listing_expiration_date": "20261231"}