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FDA Approval

OXAZEPAM

FDA-approved pharmaceutical product with comprehensive regulatory information, manufacturing details, and complete labeling documentation.

FDA Approval Summary

Company
STAT RX USA LLC
DUNS: 786036330
Effective Date
December 15, 2009
Labeling Type
HUMAN PRESCRIPTION DRUG LABEL
Oxazepam(15 mg in 1 1)

Products1

Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.

OXAZEPAM

Product Details

NDC Product Code
16590-304
Application Number
ANDA072252
Marketing Category
ANDA (C73584)
Route of Administration
ORAL
Effective Date
December 15, 2009
OxazepamActive
Code: 6GOW6DWN2AClass: ACTIBQuantity: 15 mg in 1 1
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