πΊπΈ
United States Β· US Β· US:49643-116_36ad1e17-751d-e226-e063-6394a90ab328
Phoma
UNII
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerAllermed Laboratories, Inc.
CountryUS (United States)
ATC codeβ
Dispensingβ
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs Β· 4
- ndc1149643116055 mL in 1 VIAL, MULTI-DOSE (49643-116-05)
- ndc11496431161010 mL in 1 VIAL, MULTI-DOSE (49643-116-10)
- ndc11496431163030 mL in 1 VIAL, MULTI-DOSE (49643-116-30)
- ndc11496431165050 mL in 1 VIAL, MULTI-DOSE (49643-116-50)
Annotations
UNII (FDA Substance ID)
V58BK047ES
PLEOSPORA BETAE
Raw payload (JSON)
{
"unii": {
"unii": "V58BK047ES",
"rxcui": null,
"inchikey": null,
"display_name": "PLEOSPORA BETAE",
"substance_type": "structurallyDiverse",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "CUTANEOUS; INTRADERMAL; SUBCUTANEOUS",
"productid": "49643-116_36ad1e17-751d-e226-e063-6394a90ab328",
"productndc": "49643-116",
"dosage_form": "INJECTION",
"dea_schedule": null,
"product_type": "NON-STANDARDIZED ALLERGENIC",
"substance_name": "PLEOSPORA BETAE",
"proprietary_name": "Phoma",
"active_ingred_unit": "g/mL",
"application_number": "BLA102211",
"marketing_category": "BLA",
"nonproprietary_name": "Phoma betae",
"start_marketing_date": "19740312",
"active_numerator_strength": ".1"
}Access this data programmatically
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