NDC 36987-2244

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: 36987-2244_3f71b69c-37b8-4c27-af1a-cc5178f3ff61
• NDC: 36987-2244
• 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 36987-2244-4

50 mL in 1 VIAL, MULTI-DOSE (36987-2244-4)

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

NDC SPL Data Element Entries

NDC 36987-2244-2 [36987224402]

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 36987-2244-4 [36987224404]

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 36987-2244-3 [36987224403]

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 36987-2244-1 [36987224401]

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	.025 g/mL

OpenFDA Data

• SPL SET ID: 9a0a10e2-1458-4e1a-a678-2a3863f22f5a
• Manufacturer:
  • Nelco Laboratories, Inc.
• UNII:
  • 70LDW53ROO
  • 4110YT348C
  • M30XO5X4XD
  • MRJ91HVV4H
  • DI0ZRJ0MXN
  • TVA75O7S63
  • 758Z9H9WV9
  • 6YR2608RSU
• RxNorm Concept Unique ID - RxCUI:
  • 851885
  • 966930
  • 904971
  • 852415
  • 852318
  • 889600
  • 904638
  • 966962
  • 852547

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