NDC 49288-0461

Miller Moth

Miller Moth

Miller Moth is a Intradermal; Subcutaneous Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by Antigen Laboratories, Inc.. The primary component is Sitotroga Cerealella.

Product ID49288-0461_f1a31511-6642-4da5-82cf-67c9ca728bc6
NDC49288-0461
Product TypeHuman Prescription Drug
Proprietary NameMiller Moth
Generic NameMiller Moth
Dosage FormInjection, Solution
Route of AdministrationINTRADERMAL; SUBCUTANEOUS
Marketing Start Date1974-03-23
Marketing CategoryBLA / BLA
Application NumberBLA102223
Labeler NameAntigen Laboratories, Inc.
Substance NameSITOTROGA CEREALELLA
Active Ingredient Strength0 g/mL
NDC Exclude FlagE
Listing Certified Through2017-12-31

Packaging

NDC 49288-0461-2

5 mL in 1 VIAL, MULTI-DOSE (49288-0461-2)
Marketing Start Date1974-03-23
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 49288-0461-5 [49288046105]

Miller Moth INJECTION, SOLUTION
Marketing CategoryBLA
Application NumberBLA102223
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1974-03-23
Inactivation Date2019-10-21

NDC 49288-0461-2 [49288046102]

Miller Moth INJECTION, SOLUTION
Marketing CategoryBLA
Application NumberBLA102223
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1974-03-23
Inactivation Date2019-10-21

NDC 49288-0461-3 [49288046103]

Miller Moth INJECTION, SOLUTION
Marketing CategoryBLA
Application NumberBLA102223
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1974-03-23
Inactivation Date2019-10-21

NDC 49288-0461-4 [49288046104]

Miller Moth INJECTION, SOLUTION
Marketing CategoryBLA
Application NumberBLA102223
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1974-03-23
Inactivation Date2019-10-21

NDC 49288-0461-1 [49288046101]

Miller Moth INJECTION, SOLUTION
Marketing CategoryBLA
Application NumberBLA102223
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1974-03-23
Inactivation Date2019-10-21

Drug Details

Active Ingredients

IngredientStrength
SITOTROGA CEREALELLA.05 g/mL

OpenFDA Data

SPL SET ID:9de836ec-49c1-47a2-a0c5-b9f30ae924be
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 892363

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