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United States · US · US:50090-7581_c0735e0a-75d4-43f5-9be6-3508104d4142
Ciprofloxacin
Orange BookUNIISPLATC J01MA02
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerA-S Medication Solutions
CountryUS (United States)
ATC codeJ01MA02
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11500907581020 TABLET, FILM COATED in 1 BOTTLE (50090-7581-0)
Annotations
UNII (FDA Substance ID)
4BA73M5E37
CIPROFLOXACIN HYDROCHLORIDE
RxCUI 81981
Orange Book
A076126
ABABAB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "4BA73M5E37",
"rxcui": "81981",
"inchikey": "ARPUHYJMCVWYCZ-UHFFFAOYSA-N",
"display_name": "CIPROFLOXACIN HYDROCHLORIDE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"a05035e1-f941-4f7c-9321-91dd50ab149b": {
"match": "brand_token",
"title": "CIPROFLOXACIN TABLET, COATED [BRYANT RANCH PREPACK]",
"spl_version": "104",
"published_date": "2026-06-01"
}
},
"productid": "50090-7581_c0735e0a-75d4-43f5-9be6-3508104d4142",
"productndc": "50090-7581",
"dosage_form": "TABLET, FILM COATED",
"orange_book": {
"appl_no": "076126",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "EQ 250MG BASE",
"product_no": "002",
"approval_date": "Jun 9, 2004"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "EQ 500MG BASE",
"product_no": "003",
"approval_date": "Jun 9, 2004"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "EQ 750MG BASE",
"product_no": "004",
"approval_date": "Jun 9, 2004"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "CIPROFLOXACIN HYDROCHLORIDE",
"proprietary_name": "Ciprofloxacin",
"active_ingred_unit": "mg/1",
"application_number": "ANDA076126",
"marketing_category": "ANDA",
"nonproprietary_name": "Ciprofloxacin Hydrochloride",
"start_marketing_date": "20091010",
"active_numerator_strength": "250"
}Related drugs
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