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United States · US · US:43598-632_716e99cb-d17e-d5ca-61aa-3298ab7fee96
Fluoxetine hydrochloride
Orange BookUNIISPLATC N06AB03
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerDr. Reddy's Laboratories Inc.
CountryUS (United States)
ATC codeN06AB03
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc114359863201100 TABLET, FILM COATED in 1 BOTTLE (43598-632-01)
- ndc11435986323030 TABLET, FILM COATED in 1 BOTTLE (43598-632-30)
Annotations
UNII (FDA Substance ID)
I9W7N6B1KJ
FLUOXETINE HYDROCHLORIDE
RxCUI 227224
Orange Book
A211721
AB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "I9W7N6B1KJ",
"rxcui": "227224",
"inchikey": "GIYXAJPCNFJEHY-UHFFFAOYSA-N",
"display_name": "FLUOXETINE HYDROCHLORIDE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"1a2a5194-b793-4c62-a177-040dad38526b": {
"match": "brand_token",
"title": "FLUOXETINE CAPSULE [PROFICIENT RX LP]",
"spl_version": "6",
"published_date": "2026-05-29"
}
},
"productid": "43598-632_716e99cb-d17e-d5ca-61aa-3298ab7fee96",
"productndc": "43598-632",
"dosage_form": "TABLET, FILM COATED",
"orange_book": {
"appl_no": "211721",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "EQ 60MG BASE",
"product_no": "001",
"approval_date": "Jan 25, 2019"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "FLUOXETINE HYDROCHLORIDE",
"proprietary_name": "Fluoxetine hydrochloride",
"active_ingred_unit": "mg/1",
"application_number": "ANDA211721",
"marketing_category": "ANDA",
"nonproprietary_name": "Fluoxetine hydrochloride",
"start_marketing_date": "20190128",
"active_numerator_strength": "60"
}Related drugs
Other records sharing ATC code N06AB03.
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