Product NDC: | 0456-1201 |
Proprietary Name: | Linzess |
Non Proprietary Name: | linaclotide |
Active Ingredient(s): | 145 ug/1 & nbsp; linaclotide |
Administration Route(s): | ORAL |
Dosage Form(s): | CAPSULE, GELATIN COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0456-1201 |
Labeler Name: | Forest Laboratories, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA202811 |
Marketing Category: | NDA |
Start Marketing Date: | 20120908 |
Package NDC: | 0456-1201-30 |
Package Description: | 1 BOTTLE in 1 CARTON (0456-1201-30) > 30 CAPSULE, GELATIN COATED in 1 BOTTLE |
NDC Code | 0456-1201-30 |
Proprietary Name | Linzess |
Package Description | 1 BOTTLE in 1 CARTON (0456-1201-30) > 30 CAPSULE, GELATIN COATED in 1 BOTTLE |
Product NDC | 0456-1201 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | linaclotide |
Dosage Form Name | CAPSULE, GELATIN COATED |
Route Name | ORAL |
Start Marketing Date | 20120908 |
Marketing Category Name | NDA |
Labeler Name | Forest Laboratories, Inc. |
Substance Name | LINACLOTIDE |
Strength Number | 145 |
Strength Unit | ug/1 |
Pharmaceutical Classes | Guanylate Cyclase-C Agonist [EPC],Guanylate Cyclase Activators [MoA] |