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United States · US · US:71205-474_4702c59e-202c-4900-9388-f64788cb035c
Baclofen
UNIISPLATC M03BX01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerProficient Rx LP
CountryUS (United States)
ATC codeM03BX01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 7
- ndc11712054741414 TABLET in 1 BOTTLE (71205-474-14)
- ndc11712054742020 TABLET in 1 BOTTLE (71205-474-20)
- ndc11712054743030 TABLET in 1 BOTTLE (71205-474-30)
- ndc11712054746060 TABLET in 1 BOTTLE (71205-474-60)
- ndc117120547472120 TABLET in 1 BOTTLE (71205-474-72)
- ndc117120547478180 TABLET in 1 BOTTLE (71205-474-78)
- ndc11712054749090 TABLET in 1 BOTTLE (71205-474-90)
Annotations
UNII (FDA Substance ID)
H789N3FKE8
BACLOFEN
RxCUI 1292
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "H789N3FKE8",
"rxcui": "1292",
"inchikey": "KPYSYYIEGFHWSV-UHFFFAOYSA-N",
"display_name": "BACLOFEN",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"e017a001-8cb1-4dd8-960e-c6d74005f57f": {
"match": "brand_token",
"title": "BACLOFEN TABLET [REMEDYREPACK INC.]",
"spl_version": "1",
"published_date": "2026-05-13"
}
},
"productid": "71205-474_4702c59e-202c-4900-9388-f64788cb035c",
"productndc": "71205-474",
"dosage_form": "TABLET",
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "BACLOFEN",
"proprietary_name": "Baclofen",
"active_ingred_unit": "mg/1",
"application_number": "ANDA078504",
"marketing_category": "ANDA",
"nonproprietary_name": "Baclofen",
"start_marketing_date": "20110101",
"active_numerator_strength": "10"
}Related drugs
Other records sharing ATC code M03BX01.
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