Sentraflox AM-10
These highlights do not include all the information needed to use fluoxetine capsules USP safely and effectively. See full prescribing information for fluoxetine capsules USP. Initial U.S. Approval: 1987
Approved
Approval ID
35fee753-acd7-4da2-bd60-973dc6c0b21f
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Aug 17, 2011
Manufacturers
FDA
Physician Therapeutics LLC
DUNS: 931940964
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
FLUOXETINE HYDROCHLORIDE, CHOLINE
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code68405-022
Product Classification
G
Generic Name
FLUOXETINE HYDROCHLORIDE, CHOLINE
Product Specifications
Effective DateAugust 10, 2011
FDA Product Classification