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United States · US · US:0527-1330_153f6bd7-9462-4d92-b738-48e7807c5919
Baclofen
UNIISPLATC M03BX01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerLannett Company, Inc.
CountryUS (United States)
ATC codeM03BX01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 3
- ndc110527133001100 TABLET in 1 BOTTLE, PLASTIC (0527-1330-01)
- ndc110527133005500 TABLET in 1 BOTTLE, PLASTIC (0527-1330-05)
- ndc1105271330101000 TABLET in 1 BOTTLE, PLASTIC (0527-1330-10)
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": "0527-1330_153f6bd7-9462-4d92-b738-48e7807c5919",
"productndc": "0527-1330",
"dosage_form": "TABLET",
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "BACLOFEN",
"proprietary_name": "Baclofen",
"active_ingred_unit": "mg/1",
"application_number": "ANDA078220",
"marketing_category": "ANDA",
"nonproprietary_name": "baclofen",
"start_marketing_date": "20070701",
"active_numerator_strength": "10"
}Related drugs
Other records sharing ATC code M03BX01.
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