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United States · US · US:68071-3611_1b406836-6662-90fd-e063-6294a90aaea0
Ondansetron
Orange BookUNIISPLATC A04AA01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerNuCare Pharmaceuticals,Inc.
CountryUS (United States)
ATC codeA04AA01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1168071361151 BOTTLE, PLASTIC in 1 CARTON (68071-3611-5) / 50 mL in 1 BOTTLE, PLASTIC
Annotations
UNII (FDA Substance ID)
NMH84OZK2B
ONDANSETRON HYDROCHLORIDE
RxCUI 203148
Orange Book
A078776
AA
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "NMH84OZK2B",
"rxcui": "203148",
"inchikey": "VRSLTNZJOUZKLX-UHFFFAOYSA-N",
"display_name": "ONDANSETRON HYDROCHLORIDE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"d62cd60b-f87e-4825-bead-1d18bbc4e480": {
"match": "brand_token",
"title": "ONDANSETRON INJECTION, SOLUTION [HOSPIRA, INC.]",
"spl_version": "4",
"published_date": "2026-05-25"
}
},
"productid": "68071-3611_1b406836-6662-90fd-e063-6294a90aaea0",
"productndc": "68071-3611",
"dosage_form": "SOLUTION",
"orange_book": {
"appl_no": "078776",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AA",
"strength": "EQ 4MG BASE/5ML",
"product_no": "001",
"approval_date": "Nov 28, 2007"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "ONDANSETRON HYDROCHLORIDE",
"proprietary_name": "Ondansetron",
"active_ingred_unit": "mg/5mL",
"application_number": "ANDA078776",
"marketing_category": "ANDA",
"nonproprietary_name": "Ondansetron Hydrochloride",
"start_marketing_date": "20071128",
"active_numerator_strength": "4"
}Related drugs
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- CAAPO-ONDANSETRONAPOTEX INC
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