diazepam
Generic: diazepam
Labeler: a-s medication solutionsDrug Facts
Product Profile
Brand Name
diazepam
Generic Name
diazepam
Labeler
a-s medication solutions
Dosage Form
TABLET
Routes
Active Ingredients
diazepam 2 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
50090-3390
Product ID
50090-3390_842dfa9a-8c93-4c77-8f6b-95dd175df191
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA070325
DEA Schedule
civ
Listing Expiration
2026-12-31
Marketing Start
1985-09-04
Pharmacologic Class
Established (EPC)
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
500903390
Hyphenated Format
50090-3390
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
ANDA070325 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 2 mg/1
Packaging
- 60 TABLET in 1 BOTTLE (50090-3390-1)
- 2 TABLET in 1 BOTTLE, PLASTIC (50090-3390-6)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "842dfa9a-8c93-4c77-8f6b-95dd175df191", "openfda": {"nui": ["N0000175694", "M0002356"], "unii": ["Q3JTX2Q7TU"], "rxcui": ["197590"], "spl_set_id": ["01f04ee4-fff9-499a-8213-984e16368084"], "pharm_class_cs": ["Benzodiazepines [CS]"], "pharm_class_epc": ["Benzodiazepine [EPC]"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (50090-3390-1)", "package_ndc": "50090-3390-1", "marketing_start_date": "20181008"}, {"sample": false, "description": "2 TABLET in 1 BOTTLE, PLASTIC (50090-3390-6)", "package_ndc": "50090-3390-6", "marketing_start_date": "20141128"}], "brand_name": "Diazepam", "product_id": "50090-3390_842dfa9a-8c93-4c77-8f6b-95dd175df191", "dosage_form": "TABLET", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "50090-3390", "dea_schedule": "CIV", "generic_name": "diazepam", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diazepam", "active_ingredients": [{"name": "DIAZEPAM", "strength": "2 mg/1"}], "application_number": "ANDA070325", "marketing_category": "ANDA", "marketing_start_date": "19850904", "listing_expiration_date": "20261231"}