NDC 76282-709

Lanreotide Acetate

Lanreotide Acetate

Lanreotide Acetate is a Subcutaneous Injection in the Human Prescription Drug category. It is labeled and distributed by Exelan Pharmaceuticals, Inc.. The primary component is Lanreotide Acetate.

Product ID76282-709_1eaf1cf6-23b6-4c54-8cbf-a96d1f74c4cc
NDC76282-709
Product TypeHuman Prescription Drug
Proprietary NameLanreotide Acetate
Generic NameLanreotide Acetate
Dosage FormInjection
Route of AdministrationSUBCUTANEOUS
Marketing Start Date2022-06-01
Marketing CategoryNDA /
Application NumberNDA215395
Labeler NameExelan Pharmaceuticals, Inc.
Substance NameLANREOTIDE ACETATE
Active Ingredient Strength60 mg/.2mL
Pharm ClassesSomatostatin Analog [EPC], Somatostatin Receptor Agonists [MoA]
NDC Exclude FlagN
Listing Certified Through2023-12-31

Packaging

NDC 76282-709-67

1 SYRINGE in 1 CARTON (76282-709-67) > .2 mL in 1 SYRINGE
Marketing Start Date2022-06-01
NDC Exclude FlagN
Sample Package?N

Drug Details

NDC Crossover Matching brand name "Lanreotide Acetate" or generic name "Lanreotide Acetate"

NDCBrand NameGeneric Name
69097-870Lanreotide Acetatelanreotide acetate
69097-880Lanreotide Acetatelanreotide acetate
69097-890Lanreotide Acetatelanreotide acetate
76282-709Lanreotide Acetatelanreotide acetate
76282-710Lanreotide Acetatelanreotide acetate
76282-711Lanreotide Acetatelanreotide acetate
15054-1060SOMATULINE DEPOTlanreotide acetate
15054-1090SOMATULINE DEPOTlanreotide acetate
15054-1120SOMATULINE DEPOTlanreotide acetate

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