Product NDC: | 0067-6286 |
Proprietary Name: | Prevacid |
Non Proprietary Name: | Lansoprazole |
Active Ingredient(s): | 15 mg/1 & nbsp; Lansoprazole |
Administration Route(s): | ORAL |
Dosage Form(s): | CAPSULE, DELAYED RELEASE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0067-6286 |
Labeler Name: | Novartis Consumer Health, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | NDA022327 |
Marketing Category: | NDA |
Start Marketing Date: | 20091112 |
Package NDC: | 0067-6286-14 |
Package Description: | 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE (0067-6286-14) |
NDC Code | 0067-6286-14 |
Proprietary Name | Prevacid |
Package Description | 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE (0067-6286-14) |
Product NDC | 0067-6286 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Lansoprazole |
Dosage Form Name | CAPSULE, DELAYED RELEASE |
Route Name | ORAL |
Start Marketing Date | 20091112 |
Marketing Category Name | NDA |
Labeler Name | Novartis Consumer Health, Inc. |
Substance Name | LANSOPRAZOLE |
Strength Number | 15 |
Strength Unit | mg/1 |
Pharmaceutical Classes |