49643-114 : Mucor 1 g/10ml Cutaneous; Intradermal; Subcutaneous Injection


NDC: 49643-114
Labeler: Allermed Laboratories, Inc.
Product Type: Non-standardized Allergenic
Drug Name: Mucor
Dosage Form: Cutaneous; Intradermal; Subcutaneous Injection
Application #: BLA102212
Rev. Date: 


NDC Package Codes:

  • 49643-114-05: 5 ML IN 1 VIAL, MULTI‑DOSE (49643‑114‑05)
  • 49643-114-10: 10 ML IN 1 VIAL, MULTI‑DOSE (49643‑114‑10)
  • 49643-114-30: 30 ML IN 1 VIAL, MULTI‑DOSE (49643‑114‑30)
  • 49643-114-50: 50 ML IN 1 VIAL, MULTI‑DOSE (49643‑114‑50)

Active Ingredients:

  • Mucor Racemosus

Dosage Strength:

  • .1 g/mL

Pharmaceutical Classes:

  • Allergens [CS]
  • Cell-mediated Immunity [PE]
  • Fungal Proteins [CS]
  • Increased Histamine Release [PE]
  • Increased IgG Production [PE]
  • Non-Standardized Fungal Allergenic Extract [EPC]

Related Products:

Based on records with the same trade name.
  • 49693-1301 Mucor 4 [hp_x]/10ml Oral Liquid by Uspharmaco
  • 49693-1306 Mucor 5 [hp_x]/5ml Ophthalmic Liquid by Uspharmaco

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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.