Product NDC: | 62011-0157 |
Proprietary Name: | health mart omeprazole |
Non Proprietary Name: | Omeprazole |
Active Ingredient(s): | 20 mg/1 & nbsp; Omeprazole |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, DELAYED RELEASE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 62011-0157 |
Labeler Name: | McKesson |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | NDA022032 |
Marketing Category: | NDA |
Start Marketing Date: | 20120320 |
Package NDC: | 62011-0157-1 |
Package Description: | 1 BLISTER PACK in 1 CARTON (62011-0157-1) > 14 TABLET, DELAYED RELEASE in 1 BLISTER PACK |
NDC Code | 62011-0157-1 |
Proprietary Name | health mart omeprazole |
Package Description | 1 BLISTER PACK in 1 CARTON (62011-0157-1) > 14 TABLET, DELAYED RELEASE in 1 BLISTER PACK |
Product NDC | 62011-0157 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Omeprazole |
Dosage Form Name | TABLET, DELAYED RELEASE |
Route Name | ORAL |
Start Marketing Date | 20120320 |
Marketing Category Name | NDA |
Labeler Name | McKesson |
Substance Name | OMEPRAZOLE |
Strength Number | 20 |
Strength Unit | mg/1 |
Pharmaceutical Classes |