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United States · US · US:72162-1079_5de12657-b943-4215-8979-d2a285fcd7ec
Baclofen
UNIISPLATC M03BX01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerBryant Ranch Prepack
CountryUS (United States)
ATC codeM03BX01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 4
- ndc1172162107901000 TABLET in 1 BOTTLE, PLASTIC (72162-1079-0)
- ndc117216210791100 TABLET in 1 BOTTLE, PLASTIC (72162-1079-1)
- ndc117216210798140 TABLET in 1 BOTTLE, PLASTIC (72162-1079-8)
- ndc11721621079990 TABLET in 1 BOTTLE, PLASTIC (72162-1079-9)
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": "72162-1079_5de12657-b943-4215-8979-d2a285fcd7ec",
"productndc": "72162-1079",
"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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