CHLORDIAZEPOXIDE HYDROCHLORIDE AND CLIDINIUM BROMIDE
Summary
FDA approved CHLORDIAZEPOXIDE HYDROCHLORIDE AND CLIDINIUM BROMIDE by NUVO PHARMS INC. ANDA (Generic) approval (Labeling) on 2022-08-24. CAPSULE, ORAL.
Details
Source
Drug Approval
External ID
ANDA211421-2
Action Date
2022-08-24
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
CHLORDIAZEPOXIDE HYDROCHLORIDE AND CLIDINIUM BROMIDE, CAPSULE, ORAL. Application: ANDA211421
Company
Context & Analysis
Frequently Asked Questions
How often does NUVO PHARMS INC have FDA actions?
This is the only FDA action we have on record for NUVO PHARMS INC in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "ANDA211421-2" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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