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United States · US · US:0093-2204_61b5d2d5-1e7b-44ff-a831-1a0de78edecd
Metoclopramide
Orange BookUNIISPLATC A03FA01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerTeva Pharmaceuticals USA, Inc.
CountryUS (United States)
ATC codeA03FA01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc110093220401100 TABLET in 1 BOTTLE (0093-2204-01)
- ndc110093220405500 TABLET in 1 BOTTLE (0093-2204-05)
Annotations
UNII (FDA Substance ID)
W1792A2RVD
METOCLOPRAMIDE HYDROCHLORIDE
RxCUI 267036
Orange Book
A072801
AB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "W1792A2RVD",
"rxcui": "267036",
"inchikey": "KJBLQGHJOCAOJP-UHFFFAOYSA-N",
"display_name": "METOCLOPRAMIDE HYDROCHLORIDE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"5645a752-8868-4b51-8b59-48bb4276d763": {
"match": "brand_token",
"title": "METOCLOPRAMIDE INJECTION, SOLUTION [TEVA PARENTERAL MEDICINES, INC.]",
"spl_version": "8",
"published_date": "2026-05-29"
}
},
"productid": "0093-2204_61b5d2d5-1e7b-44ff-a831-1a0de78edecd",
"productndc": "0093-2204",
"dosage_form": "TABLET",
"orange_book": {
"appl_no": "072801",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "EQ 5MG BASE",
"product_no": "001",
"approval_date": "Jun 15, 1993"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "METOCLOPRAMIDE HYDROCHLORIDE",
"proprietary_name": "Metoclopramide",
"active_ingred_unit": "mg/1",
"application_number": "ANDA072801",
"marketing_category": "ANDA",
"nonproprietary_name": "Metoclopramide",
"start_marketing_date": "19930701",
"active_numerator_strength": "5"
}Related drugs
Other records sharing ATC code A03FA01.
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