NDC 36987-1264

Smelt

Smelt

Smelt 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 Smelt.

• Product ID: 36987-1264_2266ee8c-c745-471e-845a-267f11a1c269
• NDC: 36987-1264
• Product Type: Human Prescription Drug
• Proprietary Name: Smelt
• Generic Name: Smelt
• 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: SMELT
• Active Ingredient Strength: 0 g/mL
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 36987-1264-3

30 mL in 1 VIAL, MULTI-DOSE (36987-1264-3)

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

NDC SPL Data Element Entries

NDC 36987-1264-4 [36987126404]

Smelt 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 36987-1264-2 [36987126402]

Smelt 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 36987-1264-3 [36987126403]

Smelt 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 36987-1264-1 [36987126401]

Smelt 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
SMELT	.1 g/mL

OpenFDA Data

• SPL SET ID: ed374a8c-81d6-4389-b77b-00e5517ada89
• Manufacturer:
  • Nelco Laboratories, Inc.
• UNII:
  • BKZ683617P
  • 76780GX08D
  • 7062I37LB3
  • ZB2SV6JJY5
  • 0WLY635722
  • 01695YPV36
  • WF621S7K14
  • 5JKY494U4L
• RxNorm Concept Unique ID - RxCUI:
  • 905479
  • 892506
  • 905345
  • 892564
  • 904543
  • 901282
  • 892595
  • 892546
  • 966805
  • 899433
  • 966978
  • 901375
  • 904599
  • 901290
  • 899751
  • 899937
  • 905489
  • 901397
  • 905329
  • 892542
  • 905365
  • 892613

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

NDC	Brand Name	Generic Name
36987-1262	Smelt	Smelt
36987-1263	Smelt	Smelt
36987-1264	Smelt	Smelt
36987-1265	Smelt	Smelt