Orris Root

Last synced from FDA National Drug Code directory (United States) on June 3, 2026

Identification

ManufacturerAllermed Laboratories, Inc.

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 4

ndc11
4964302005
5 mL in 1 VIAL, MULTI-DOSE (49643-020-05)
ndc11
4964302010
10 mL in 1 VIAL, MULTI-DOSE (49643-020-10)
ndc11
4964302030
30 mL in 1 VIAL, MULTI-DOSE (49643-020-30)
ndc11
4964302050
50 mL in 1 VIAL, MULTI-DOSE (49643-020-50)

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Raw payload (JSON)

{
  "route": "CUTANEOUS; INTRADERMAL; SUBCUTANEOUS",
  "productid": "49643-020_36ad1e17-751d-e226-e063-6394a90ab328",
  "productndc": "49643-020",
  "dosage_form": "INJECTION",
  "dea_schedule": null,
  "product_type": "NON-STANDARDIZED ALLERGENIC",
  "substance_name": "IRIS GERMANICA VAR. FLORENTINA ROOT",
  "proprietary_name": "Orris Root",
  "active_ingred_unit": "g/mL",
  "application_number": "BLA102211",
  "marketing_category": "BLA",
  "nonproprietary_name": "Orris Root",
  "start_marketing_date": "19740312",
  "active_numerator_strength": ".1"
}

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