diazepam
Generic: diazepam
Labeler: proficient rx lpDrug Facts
Product Profile
Brand Name
diazepam
Generic Name
diazepam
Labeler
proficient rx lp
Dosage Form
TABLET
Routes
Active Ingredients
diazepam 10 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
63187-544
Product ID
63187-544_aeef8cde-a187-453e-b7fb-e179493ff427
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)
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
63187544
Hyphenated Format
63187-544
Supplemental Identifiers
RxCUI
UPC
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
ANDA071322 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/1
Packaging
- 6 TABLET in 1 BOTTLE (63187-544-06)
- 15 TABLET in 1 BOTTLE (63187-544-15)
- 20 TABLET in 1 BOTTLE (63187-544-20)
- 30 TABLET in 1 BOTTLE (63187-544-30)
- 60 TABLET in 1 BOTTLE (63187-544-60)
- 90 TABLET in 1 BOTTLE (63187-544-90)
Packages (6)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "aeef8cde-a187-453e-b7fb-e179493ff427", "openfda": {"nui": ["N0000175694", "M0002356"], "upc": ["0363187544300"], "unii": ["Q3JTX2Q7TU"], "rxcui": ["197589"], "spl_set_id": ["f8d26f65-a015-4bfc-b1fa-8595d72af48c"], "pharm_class_cs": ["Benzodiazepines [CS]"], "pharm_class_epc": ["Benzodiazepine [EPC]"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "6 TABLET in 1 BOTTLE (63187-544-06)", "package_ndc": "63187-544-06", "marketing_start_date": "20191217"}, {"sample": false, "description": "15 TABLET in 1 BOTTLE (63187-544-15)", "package_ndc": "63187-544-15", "marketing_start_date": "20181201"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE (63187-544-20)", "package_ndc": "63187-544-20", "marketing_start_date": "20181201"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (63187-544-30)", "package_ndc": "63187-544-30", "marketing_start_date": "20181201"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (63187-544-60)", "package_ndc": "63187-544-60", "marketing_start_date": "20181201"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (63187-544-90)", "package_ndc": "63187-544-90", "marketing_start_date": "20181201"}], "brand_name": "Diazepam", "product_id": "63187-544_aeef8cde-a187-453e-b7fb-e179493ff427", "dosage_form": "TABLET", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "63187-544", "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": "ANDA071322", "marketing_category": "ANDA", "marketing_start_date": "19861210", "listing_expiration_date": "20261231"}