NDC 36987-1156

Lamb

Lamb

Lamb 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 Lamb.

• Product ID: 36987-1156_9260de65-5d7a-40ad-b190-f4e2996a2726
• NDC: 36987-1156
• Product Type: Human Prescription Drug
• Proprietary Name: Lamb
• Generic Name: Lamb
• 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: LAMB
• Active Ingredient Strength: 0 g/mL
• Pharm Classes: Non-Standardized Food Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Allergens [CS],Dietary Proteins [CS],Meat Proteins [EXT]
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 36987-1156-2

10 mL in 1 VIAL, MULTI-DOSE (36987-1156-2)

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

NDC SPL Data Element Entries

NDC 36987-1156-3 [36987115603]

Lamb 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 36987-1156-2 [36987115602]

Lamb 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 36987-1156-1 [36987115601]

Lamb 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 36987-1156-4 [36987115604]

Lamb 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
LAMB	.1 g/mL

OpenFDA Data

• SPL SET ID: fe8288dd-c8e3-442b-a7ad-700719b3ca1a
• Manufacturer:
  • Nelco Laboratories, Inc.
• UNII:
  • 4IPS17B70T
  • O138UB266J
  • 4PIB2155QP
  • 0X5GW3050M
  • 3E0I92Z2GR
  • 291P45F896
  • 28ON068RWM
  • 0X8Q245Y7B
  • 8E9NT44R8I
  • FOF26T73HA
• RxNorm Concept Unique ID - RxCUI:
  • 966651
  • 966674
  • 1012031
  • 892656
  • 904491
  • 966647
  • 904587
  • 905323
  • 892602
  • 892631
  • 905514

Pharmacological Class

• Non-Standardized Food Allergenic Extract [EPC]
• Increased Histamine Release [PE]
• Cell-mediated Immunity [PE]
• Allergens [CS]
• Dietary Proteins [CS]
• Meat Proteins [EXT]

NDC Crossover Matching brand name "Lamb" or generic name "Lamb"

NDC	Brand Name	Generic Name
0268-6149	LAMB	Lamb
22840-5758	Lamb	Ovis aries
36987-1154	Lamb	Lamb
36987-1155	Lamb	Lamb
36987-1156	Lamb	Lamb
36987-1157	Lamb	Lamb
49288-0287	Lamb	Lamb