Fluoxetine

Product NDC
68071-4653
11-digit product format
680714653
Labeler code
68071
Product ID
68071-4653_84a066bc-e604-d470-e053-2a91aa0ab64f
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Fluoxetine Hydrochloride
Dosage form
CAPSULE
Route
ORAL
Labeler
NuCare Pharmaceuticals,Inc.
Application
ANDA204597
Marketing category
ANDA
Marketing start
2015-03-16
Marketing end
0000-00-00
Substance
FLUOXETINE HYDROCHLORIDE
Active strength
10 mg/1
Pharmacologic classes
Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
68071-4653-32024-06-12C16284748780-1ba0f9c33-303c-a910-e053-dadaa90a0b857c5e4d8e-4c69-ca0e-e053-2991aa0a5469
68071-4653-32021-01-29C16284748780-1ba0f9c33-303c-a910-e053-dadaa90a0b857c5e4d8e-4c69-ca0e-e053-2991aa0a5469