oxazepam
Generic: oxazepam
Labeler: american health packagingDrug Facts
Product Profile
Brand Name
oxazepam
Generic Name
oxazepam
Labeler
american health packaging
Dosage Form
CAPSULE, GELATIN COATED
Routes
Active Ingredients
oxazepam 10 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
62584-812
Product ID
62584-812_26e63053-7a43-e278-e063-6394a90a23b8
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA072253
DEA Schedule
civ
Listing Expiration
2026-12-31
Marketing Start
2007-12-17
Pharmacologic Class
Established (EPC)
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
62584812
Hyphenated Format
62584-812
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
oxazepam (source: ndc)
Generic Name
oxazepam (source: ndc)
Application Number
ANDA072253 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/1
Packaging
- 100 BLISTER PACK in 1 CARTON (62584-812-01) / 1 CAPSULE, GELATIN COATED in 1 BLISTER PACK (62584-812-11)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "26e63053-7a43-e278-e063-6394a90a23b8", "openfda": {"nui": ["N0000175694", "M0002356"], "unii": ["6GOW6DWN2A"], "rxcui": ["198057", "198059", "312134"], "spl_set_id": ["03440821-831c-4085-98f9-faa88e98c503"], "pharm_class_cs": ["Benzodiazepines [CS]"], "pharm_class_epc": ["Benzodiazepine [EPC]"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (62584-812-01) / 1 CAPSULE, GELATIN COATED in 1 BLISTER PACK (62584-812-11)", "package_ndc": "62584-812-01", "marketing_start_date": "20071217"}], "brand_name": "Oxazepam", "product_id": "62584-812_26e63053-7a43-e278-e063-6394a90a23b8", "dosage_form": "CAPSULE, GELATIN COATED", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "62584-812", "dea_schedule": "CIV", "generic_name": "Oxazepam", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxazepam", "active_ingredients": [{"name": "OXAZEPAM", "strength": "10 mg/1"}], "application_number": "ANDA072253", "marketing_category": "ANDA", "marketing_start_date": "20071217", "listing_expiration_date": "20261231"}