diazepam
Generic: diazepam
Labeler: oceanside pharmaceuticalsDrug Facts
Product Profile
Brand Name
diazepam
Generic Name
diazepam
Labeler
oceanside pharmaceuticals
Dosage Form
GEL
Routes
Active Ingredients
diazepam 10 mg/2mL
Manufacturer
Identifiers & Regulatory
Product NDC
68682-652
Product ID
68682-652_0e23d654-d8b9-af1c-e063-6294a90a6f14
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA AUTHORIZED GENERIC
Application Number
NDA020648
DEA Schedule
civ
Listing Expiration
2026-12-31
Marketing Start
1997-07-29
Pharmacologic Class
Established (EPC)
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
68682652
Hyphenated Format
68682-652
Supplemental Identifiers
RxCUI
UNII
NUI
Packaging Origin
Original Packager
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
NDA020648 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/2mL
Packaging
- 2 SYRINGE, PLASTIC in 1 PACKAGE (68682-652-20) / 2 mL in 1 SYRINGE, PLASTIC
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["RECTAL"], "spl_id": "0e23d654-d8b9-af1c-e063-6294a90a6f14", "openfda": {"nui": ["N0000175694", "M0002356"], "unii": ["Q3JTX2Q7TU"], "rxcui": ["801957", "801961", "801966"], "spl_set_id": ["b1b2848b-b265-4f6f-9141-bf106dec0726"], "pharm_class_cs": ["Benzodiazepines [CS]"], "pharm_class_epc": ["Benzodiazepine [EPC]"], "manufacturer_name": ["Oceanside Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 SYRINGE, PLASTIC in 1 PACKAGE (68682-652-20) / 2 mL in 1 SYRINGE, PLASTIC", "package_ndc": "68682-652-20", "marketing_start_date": "19970729"}], "brand_name": "Diazepam", "product_id": "68682-652_0e23d654-d8b9-af1c-e063-6294a90a6f14", "dosage_form": "GEL", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "68682-652", "dea_schedule": "CIV", "generic_name": "diazepam", "labeler_name": "Oceanside Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diazepam", "active_ingredients": [{"name": "DIAZEPAM", "strength": "10 mg/2mL"}], "application_number": "NDA020648", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "19970729", "listing_expiration_date": "20261231"}