NDC 36987-2706

Rocky Mountain Juniper

Rocky Mountain Juniper

Rocky Mountain Juniper 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 Juniperus Scopulorum Pollen.

• Product ID: 36987-2706_ca9dfb3b-60b5-4a0b-83ff-990c5959c205
• NDC: 36987-2706
• Product Type: Human Prescription Drug
• Proprietary Name: Rocky Mountain Juniper
• Generic Name: Rocky Mountain Juniper
• 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: JUNIPERUS SCOPULORUM POLLEN
• Active Ingredient Strength: 0 g/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 36987-2706-4

50 mL in 1 VIAL, MULTI-DOSE (36987-2706-4)

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

NDC SPL Data Element Entries

NDC 36987-2706-1 [36987270601]

Rocky Mountain Juniper 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 36987-2706-4 [36987270604]

Rocky Mountain Juniper 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 36987-2706-3 [36987270603]

Rocky Mountain Juniper 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 36987-2706-2 [36987270602]

Rocky Mountain Juniper 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
JUNIPERUS SCOPULORUM POLLEN	.05 g/mL

OpenFDA Data

• SPL SET ID: 40e787f4-4eef-40de-be33-86ab7b36f0f3
• 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:
  • 852672
  • 851905
  • 852753
  • 852572
  • 851913
  • 851869
  • 900734
  • 852656
  • 851739
  • 851917
  • 1006374
  • 900994
  • 900048
  • 1044349
  • 852181
  • 1111027
  • 852741
  • 852342
  • 852263
  • 852453
  • 852712
  • 895356
  • 852612
  • 852224
  • 852630
  • 852305
  • 889650
  • 900773
  • 852600
  • 900116
  • 1014363
  • 852323
  • 1115265
  • 852817
  • 852422
  • 852173
  • 852284
  • 903916
  • 901025
  • 852177
  • 897406
  • 852151
  • 852297
  • 1013964
  • 1013916
  • 851747
  • 852366
  • 852604
  • 851743
  • 1299985
  • 852499
  • 852057
  • 851877
  • 852385
  • 899596
  • 852719
  • 852584
  • 1014194
  • 1044329
  • 852275
  • 852351
  • 852379
  • 852271
  • 852232
  • 852196
  • 852564
  • 995757
  • 852358
  • 852279
  • 852809
  • 852370
  • 900111
  • 852592
  • 900746
  • 852683
  • 867300
  • 898012
  • 852749
  • 852165
  • 852580
  • 852147
  • 852625
  • 901018
  • 852143

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 "Rocky Mountain Juniper" or generic name "Rocky Mountain Juniper"

NDC	Brand Name	Generic Name
36987-2701	Rocky Mountain Juniper	Rocky Mountain Juniper
36987-2702	Rocky Mountain Juniper	Rocky Mountain Juniper
36987-2703	Rocky Mountain Juniper	Rocky Mountain Juniper
36987-2704	Rocky Mountain Juniper	Rocky Mountain Juniper
36987-2705	Rocky Mountain Juniper	Rocky Mountain Juniper
36987-2706	Rocky Mountain Juniper	Rocky Mountain Juniper
36987-2707	Rocky Mountain Juniper	Rocky Mountain Juniper
36987-2708	Rocky Mountain Juniper	Rocky Mountain Juniper