NDC 36987-2062

Phoma glomerata

Phoma Glomerata

Phoma glomerata 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 Phoma Glomerata.

• Product ID: 36987-2062_9ea18f57-b968-4c63-84f4-9e6ae475d10f
• NDC: 36987-2062
• Product Type: Human Prescription Drug
• Proprietary Name: Phoma glomerata
• Generic Name: Phoma Glomerata
• 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: PHOMA GLOMERATA
• Active Ingredient Strength: 0 g/mL
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 36987-2062-3

30 mL in 1 VIAL, MULTI-DOSE (36987-2062-3)

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

NDC SPL Data Element Entries

NDC 36987-2062-4 [36987206204]

Phoma glomerata 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 36987-2062-3 [36987206203]

Phoma glomerata 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 36987-2062-2 [36987206202]

Phoma glomerata 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 36987-2062-1 [36987206201]

Phoma glomerata 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
PHOMA GLOMERATA	.1 g/mL

OpenFDA Data

• SPL SET ID: 3484572a-db45-479f-8ba4-39a9d1b00d04
• Manufacturer:
  • Nelco Laboratories, Inc.
• UNII:
  • 3F36V0451W
  • D1A2NG69CK
  • 2072U60DUI
  • 62TY3X4N9Z
  • 3Y1PE1GCIG
  • TGO054E31O
  • 4K7Z7K7SWG
  • V4OQR60A5P
  • UPX000VMIF
  • TBW53313S7
  • C7000B9PQI
  • BV82OL2IZ8
  • 978D8U419H
  • 3LN5B70U4W
  • QBN8K7055X
  • O0HJ02QBWN
  • 87U156LEN7
  • 49W168AES4
  • X88DF51T48
  • 199I7J3JIV
  • 5016WB8B8A
  • CA33Q4013Q
  • 5964J742O8
  • 3J888Y9L13
  • 4ZWY20GTGO
  • 8476849N1Y
  • 9IOA40ANG6
  • 52B29REC7H
  • XQ14H1462M
  • YIH315U1TU
  • W042YAB8JC
  • 4D7G21HDBC
  • D7401PWY6E
• RxNorm Concept Unique ID - RxCUI:
  • 854133
  • 892677
  • 852469
  • 1006326
  • 852105
  • 968480
  • 852401
  • 1012148
  • 1011991
  • 852375
  • 968143
  • 1010906
  • 967949
  • 967869
  • 901848
  • 889542
  • 852763
  • 968210
  • 1006290
  • 967534
  • 905075
  • 1012033
  • 852192
  • 968448
  • 966685
  • 889587
  • 889620
  • 995697
  • 1012102
  • 852060
  • 967053
  • 967032
  • 1012043
• Pharm Class PE:
  • Cell-mediated Immunity [PE]
  • Increased IgG Production [PE]
  • Increased Histamine Release [PE]
• PHarm Class EPC:
  • Non-Standardized Fungal Allergenic Extract [EPC]
• NUI Code:
  • N0000185001
  • N0000175629
  • N0000171131
  • N0000185372
  • N0000169106
  • N0000184306

NDC Crossover Matching brand name "Phoma glomerata" or generic name "Phoma Glomerata"

NDC	Brand Name	Generic Name
36987-2055	Phoma glomerata	Phoma glomerata
36987-2056	Phoma glomerata	Phoma glomerata
36987-2057	Phoma glomerata	Phoma glomerata
36987-2058	Phoma glomerata	Phoma glomerata
36987-2059	Phoma glomerata	Phoma glomerata
36987-2060	Phoma glomerata	Phoma glomerata
36987-2061	Phoma glomerata	Phoma glomerata
36987-2062	Phoma glomerata	Phoma glomerata
36987-2063	Phoma glomerata	Phoma glomerata