ATROPINE SULFATE
Summary
FDA approved ATROPINE SULFATE by BAUSCH AND LOMB INC. NDA (New Drug) approval (Type 5 - New Formulation or New Manufacturer) on 2022-03-15. SOLUTION/DROPS, OPHTHALMIC.
Details
Source
Drug Approval
External ID
NDA213581-1
Action Date
2022-03-15
Status
Approved
Category
drug
Product Code
NDA (New Drug)
Product Description
ATROPINE SULFATE, SOLUTION/DROPS, OPHTHALMIC. Application: NDA213581
Company
Context & Analysis
BAUSCH AND LOMB INC has 5 FDA actions in our database.
Frequently Asked Questions
How often does BAUSCH AND LOMB INC have FDA actions?
BAUSCH AND LOMB INC has 5 FDA actions in our database, including 0 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "NDA213581-1" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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