NDC 36987-2889

Water Oak

Water Oak

Water Oak 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 Quercus Nigra Pollen.

• Product ID: 36987-2889_2a72f629-5585-48e0-bd3f-7804035e57fb
• NDC: 36987-2889
• Product Type: Human Prescription Drug
• Proprietary Name: Water Oak
• Generic Name: Water Oak
• 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: QUERCUS NIGRA POLLEN
• Active Ingredient Strength: 40000 [PNU]/mL
• Pharm Classes: Non-Standardized Pollen Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Pollen [CS],Allergens [CS]
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 36987-2889-1

5 mL in 1 VIAL, MULTI-DOSE (36987-2889-1)

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

NDC SPL Data Element Entries

NDC 36987-2889-4 [36987288904]

Water Oak 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 36987-2889-2 [36987288902]

Water Oak 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 36987-2889-3 [36987288903]

Water Oak 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 36987-2889-1 [36987288901]

Water Oak 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
QUERCUS NIGRA POLLEN	40000 [PNU]/mL

OpenFDA Data

• SPL SET ID: 9e44c782-6ad1-4e86-b333-e9358cbc5867
• Manufacturer:
  • Nelco Laboratories, Inc.
• UNII:
  • 928OC2TJDA
  • E03U1K03LK
  • 3MDX759C0W
  • 700NK45C76
  • Z0F2YK1B7H
  • 2147EPR64I
  • 59WAV8G5X5
  • 3I9T68187H
  • 8003NOJ82F
  • E4CG5Q55M1
  • 5Q246DS5BS
  • E3A7U1HWIO
  • G2A764T54B
  • 43R41XZ627
  • QJB9OQO689
  • G82398SD3I
  • E2B4Q4BXJG
  • TX1ER5UV3T
  • 15L060HV8H
  • P6K070AR8V
  • 0U790UB32K
  • 7JWJ3HXZ9U
  • LC8MEV9S89
  • 89BAT511BD
  • 6M2JIH93ZN
  • O12H03B41R
  • 232DMH0XVF
  • 23H70FYJ5U
  • 5928LJ1441
  • 95447163DG
  • HGH5K3653K
  • G684LX721Q
  • 68P4F4M6VD
  • ZGS382Y3AV
  • 426RHB4302
  • VOT5MA71M7
  • 34X886W1H4
  • 9LYI4RTZ52
  • 0G82TT8ZFY
  • PYO4JR720Y
  • 57BTU4547U
  • 84ZOM591BB
  • NX974IRT8E
  • 0MGE63QPFJ
  • VU8C8SB23P
  • ER172J09FM
  • PY0JA16R2G
  • Y3FRX92Z0E
  • Z4Y9ZSV4KK
  • 4O1FFR8ARN
  • 93963RFO1P
  • JQ5HI5004M
  • S8A4X05W7J
  • 1FH355G8HF
  • 9HC15X34LX
  • 96LRW14765
  • 6U600U1326
  • 476DVV63WP
  • 6EIJ3D04MR
  • 030R993R8E
  • OZJ4OE173N
  • 8KDG09A4GO
  • PM6E3FG1QK
  • 544F8MEY0Y
  • BS3OW0RZ4K
  • SVW19ET93C
  • LJT6I6Z8FD
  • 605T96G8Y5
  • ARW43087I1
  • 43IR7KR479
  • 7X8HL8GRTM
  • 1BV28146ZR
  • 808UWJ59FI
  • 51I6N3XIML
  • M0G28FH9K1
  • BWC8DYU8OS
  • 54UN9R2798
  • 02RVY6X9EC
  • V38QUQ7861
  • 042SUA2DS9
  • 7XW7TB10X9
  • P6818UI2E4
  • 294L626TT0
• RxNorm Concept Unique ID - RxCUI:
  • 1014726
  • 1045589
  • 1014337
  • 900006
  • 1232601
  • 1014720
  • 1300002
  • 900905
  • 1115281
  • 1013904
  • 1232614
  • 889556
  • 1014359
  • 1014765
  • 1014313
  • 900859
  • 1232580
  • 899572
  • 1013889
  • 899769
  • 900058
  • 900077
  • 1232597
  • 900942
  • 899590
  • 1014703
  • 1045597
  • 1193018
  • 889639
  • 1013961
  • 899604
  • 895710
  • 900036
  • 1046211
  • 1013871
  • 1013953
  • 900960
  • 899680
  • 900091
  • 895687
  • 1046217
  • 1232576
  • 899962
  • 899781
  • 1045602
  • 1232599
  • 1014686
  • 1014326
  • 1006478
  • 1193022
  • 1045583
  • 1013912
  • 895364
  • 899563
  • 899636
  • 1014225
  • 900042
  • 1014773
  • 1014724
  • 1045587
  • 1193026
  • 1014730
  • 900722
  • 1014307
  • 1115829
  • 889628
  • 1046209
  • 895457
  • 1045632
  • 895604
  • 895380
  • 1013875
  • 895700
  • 900742
  • 992836
  • 899970
  • 1045595
  • 1115835
  • 895396
  • 1045591
  • 899692
  • 900122
  • 901033
  • 895476

Pharmacological Class

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

NDC Crossover Matching brand name "Water Oak" or generic name "Water Oak"

NDC	Brand Name	Generic Name
36987-2885	Water Oak	Water Oak
36987-2886	Water Oak	Water Oak
36987-2887	Water Oak	Water Oak
36987-2888	Water Oak	Water Oak
36987-2889	Water Oak	Water Oak
36987-2890	Water Oak	Water Oak
36987-2891	Water Oak	Water Oak
36987-2892	Water Oak	Water Oak