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United States · US · US:11980-779_4ba88457-b1b2-4bbc-b086-a2bab56752a0
OCUFLOX
Orange BookUNIISPLATC J01MA01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerAllergan, Inc.
CountryUS (United States)
ATC codeJ01MA01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1111980779051 BOTTLE, DROPPER in 1 CARTON (11980-779-05) / 5 mL in 1 BOTTLE, DROPPER
Annotations
UNII (FDA Substance ID)
A4P49JAZ9H
OFLOXACIN
RxCUI 7623
Orange Book
N019921
AT
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "A4P49JAZ9H",
"rxcui": "7623",
"inchikey": "GSDSWSVVBLHKDQ-UHFFFAOYSA-N",
"display_name": "OFLOXACIN",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "OPHTHALMIC",
"spl_meta": {
"7aab4449-3dda-4e2c-8e40-b3244a548bf5": {
"match": "brand_token",
"title": "OCUFLOX (OFLOXACIN) SOLUTION/ DROPS [ALLERGAN, INC.]",
"spl_version": "13",
"published_date": "2025-01-09"
}
},
"productid": "11980-779_4ba88457-b1b2-4bbc-b086-a2bab56752a0",
"productndc": "11980-779",
"dosage_form": "SOLUTION/ DROPS",
"orange_book": {
"appl_no": "019921",
"products": [
{
"rs": true,
"rld": true,
"te_code": "AT",
"strength": "0.3%",
"product_no": "001",
"approval_date": "Jul 30, 1993"
}
],
"appl_type": "N"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "OFLOXACIN",
"proprietary_name": "OCUFLOX",
"active_ingred_unit": "mg/mL",
"application_number": "NDA019921",
"marketing_category": "NDA",
"nonproprietary_name": "ofloxacin",
"start_marketing_date": "19930801",
"active_numerator_strength": "3"
}Related drugs
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