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United States · US · US:71335-0344_8858eea4-a4da-4add-8f5e-bb264c8e85e8
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 · 10
- ndc117133503440112 TABLET in 1 BOTTLE, PLASTIC (71335-0344-0)
- ndc11713350344130 TABLET in 1 BOTTLE, PLASTIC (71335-0344-1)
- ndc117133503442120 TABLET in 1 BOTTLE, PLASTIC (71335-0344-2)
- ndc11713350344320 TABLET in 1 BOTTLE, PLASTIC (71335-0344-3)
- ndc11713350344460 TABLET in 1 BOTTLE, PLASTIC (71335-0344-4)
- ndc117133503445100 TABLET in 1 BOTTLE, PLASTIC (71335-0344-5)
- ndc11713350344656 TABLET in 1 BOTTLE, PLASTIC (71335-0344-6)
- ndc11713350344790 TABLET in 1 BOTTLE, PLASTIC (71335-0344-7)
- ndc117133503448140 TABLET in 1 BOTTLE, PLASTIC (71335-0344-8)
- ndc11713350344984 TABLET in 1 BOTTLE, PLASTIC (71335-0344-9)
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": "71335-0344_8858eea4-a4da-4add-8f5e-bb264c8e85e8",
"productndc": "71335-0344",
"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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