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United States · US · US:0093-2203_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 · 3
- ndc110093220301100 TABLET in 1 BOTTLE (0093-2203-01)
- ndc110093220305500 TABLET in 1 BOTTLE (0093-2203-05)
- ndc1100932203101000 TABLET in 1 BOTTLE (0093-2203-10)
Annotations
UNII (FDA Substance ID)
W1792A2RVD
METOCLOPRAMIDE HYDROCHLORIDE
RxCUI 267036
Orange Book
A070184
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": "0093-2203_61b5d2d5-1e7b-44ff-a831-1a0de78edecd",
"productndc": "0093-2203",
"dosage_form": "TABLET",
"orange_book": {
"appl_no": "070184",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "EQ 10MG BASE",
"product_no": "001",
"approval_date": "Jul 29, 1985"
}
],
"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": "ANDA070184",
"marketing_category": "ANDA",
"nonproprietary_name": "Metoclopramide",
"start_marketing_date": "19900930",
"active_numerator_strength": "10"
}Related drugs
Other records sharing ATC code A03FA01.
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