NDC 36987-3277

California Mugwort

California Mugwort

California Mugwort is a Intradermal; Subcutaneous Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by Nelco Laboratories, Inc.. The primary component is Artemisia Douglasiana Pollen.

• Product ID: 36987-3277_903c0001-3108-4d4a-af2c-1404cd7a36d7
• NDC: 36987-3277
• Product Type: Human Prescription Drug
• Proprietary Name: California Mugwort
• Generic Name: California Mugwort
• Dosage Form: Injection, Solution
• Route of Administration: INTRADERMAL; SUBCUTANEOUS
• Marketing Start Date: 1972-08-29
• Marketing Category: BLA / BLA
• Application Number: BLA102192
• Labeler Name: Nelco Laboratories, Inc.
• Substance Name: ARTEMISIA DOUGLASIANA POLLEN
• Active Ingredient Strength: 10000 [PNU]/mL
• Pharm Classes: Non-Standardized Pollen Allergenic Extract [EPC],Increased Histamine Release [PE],Increased IgG Production [PE],Pollen [CS],Allergens [CS],Cell-mediated Immunity [PE]
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 36987-3277-1

5 mL in 1 VIAL, MULTI-DOSE (36987-3277-1)

• Marketing Start Date: 1972-08-29
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 36987-3277-2 [36987327702]

California Mugwort INJECTION, SOLUTION

• Marketing Category: BLA
• Application Number: BLA102192
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 1972-08-29
• Inactivation Date: 2019-10-21

NDC 36987-3277-1 [36987327701]

California Mugwort INJECTION, SOLUTION

• Marketing Category: BLA
• Application Number: BLA102192
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 1972-08-29
• Inactivation Date: 2019-10-21

NDC 36987-3277-3 [36987327703]

California Mugwort INJECTION, SOLUTION

• Marketing Category: BLA
• Application Number: BLA102192
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 1972-08-29
• Inactivation Date: 2019-10-21

NDC 36987-3277-4 [36987327704]

California Mugwort INJECTION, SOLUTION

• Marketing Category: BLA
• Application Number: BLA102192
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 1972-08-29
• Inactivation Date: 2019-10-21

Drug Details

Active Ingredients

Ingredient	Strength
ARTEMISIA DOUGLASIANA POLLEN	10000 [PNU]/mL

OpenFDA Data

• SPL SET ID: 3a6d39b2-654e-4562-b632-b305be50c7fd
• Manufacturer:
  • Nelco Laboratories, Inc.
• UNII:
  • K1301R7883
• RxNorm Concept Unique ID - RxCUI:
  • 894818

Pharmacological Class

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

NDC Crossover Matching brand name "California Mugwort" or generic name "California Mugwort"

NDC	Brand Name	Generic Name
36987-3277	California Mugwort	California Mugwort
36987-3278	California Mugwort	California Mugwort
36987-3279	California Mugwort	California Mugwort
36987-3280	California Mugwort	California Mugwort
36987-3281	California Mugwort	California Mugwort
36987-3282	California Mugwort	California Mugwort
36987-3283	California Mugwort	California Mugwort
36987-3284	California Mugwort	California Mugwort