NDC 36987-2242

Tobacco Leaf

Tobacco Leaf

Tobacco Leaf 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 Tobacco Leaf.

• Product ID: 36987-2242_ec73bb3c-d08d-4a3b-92a9-d2bfd09da169
• NDC: 36987-2242
• Product Type: Human Prescription Drug
• Proprietary Name: Tobacco Leaf
• Generic Name: Tobacco Leaf
• 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: TOBACCO LEAF
• Active Ingredient Strength: 0 g/mL
• Pharm Classes: Non-Standardized Plant Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Allergens [CS],Plant Proteins [CS]
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 36987-2242-3

30 mL in 1 VIAL, MULTI-DOSE (36987-2242-3)

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

NDC SPL Data Element Entries

NDC 36987-2242-4 [36987224204]

Tobacco Leaf 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 36987-2242-3 [36987224203]

Tobacco Leaf 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 36987-2242-2 [36987224202]

Tobacco Leaf 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 36987-2242-1 [36987224201]

Tobacco Leaf 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
TOBACCO LEAF	.05 g/mL

OpenFDA Data

• SPL SET ID: 0fb71326-54c9-4139-befe-06ca832d02c8
• Manufacturer:
  • Nelco Laboratories, Inc.
• UNII:
  • 70LDW53ROO
  • 4110YT348C
  • M30XO5X4XD
  • MRJ91HVV4H
  • DI0ZRJ0MXN
  • TVA75O7S63
  • 758Z9H9WV9
  • 6YR2608RSU
• RxNorm Concept Unique ID - RxCUI:
  • 904846
  • 889598
  • 966928
  • 1098356
  • 904681
  • 966958
  • 978958
  • 904965
  • 1014199

Pharmacological Class

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

NDC Crossover Matching brand name "Tobacco Leaf" or generic name "Tobacco Leaf"

NDC	Brand Name	Generic Name
36987-2238	Tobacco Leaf	Tobacco Leaf
36987-2239	Tobacco Leaf	Tobacco Leaf
36987-2240	Tobacco Leaf	Tobacco Leaf
36987-2242	Tobacco Leaf	Tobacco Leaf
36987-2244	Tobacco Leaf	Tobacco Leaf
36987-2245	Tobacco Leaf	Tobacco Leaf
49643-022	Tobacco Leaf	Tobacco Leaf
58264-0322	A-30	TOBACCO LEAF
64117-993	Motion Sickness 1	TOBACCO LEAF
0220-4906	Tabacum	TOBACCO LEAF
0220-4907	Tabacum	TOBACCO LEAF
0220-4908	Tabacum	TOBACCO LEAF
0220-4909	Tabacum	TOBACCO LEAF
0220-4910	Tabacum	TOBACCO LEAF
0220-4911	Tabacum	TOBACCO LEAF
0220-4916	Tabacum	TOBACCO LEAF
68428-661	Tabacum	TOBACCO LEAF