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up and up omeprazole
up and up omeprazole - 11673-915-55 - (Omeprazole)
Drug Information of up and up omeprazole
| Product NDC: | 11673-915 |
| Proprietary Name: | up and up 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) |
Labeler Information of up and up omeprazole
| Product NDC: | 11673-915 |
| Labeler Name: | Target Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | NDA022032 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20090714 |
Package Information of up and up omeprazole
| Package NDC: | 11673-915-55 |
| Package Description: | 3 CARTON in 1 CARTON (11673-915-55) > 1 BLISTER PACK in 1 CARTON > 14 TABLET, DELAYED RELEASE in 1 BLISTER PACK |
NDC Information of up and up omeprazole
| NDC Code | 11673-915-55 |
| Proprietary Name | up and up omeprazole |
| Package Description | 3 CARTON in 1 CARTON (11673-915-55) > 1 BLISTER PACK in 1 CARTON > 14 TABLET, DELAYED RELEASE in 1 BLISTER PACK |
| Product NDC | 11673-915 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Omeprazole |
| Dosage Form Name | TABLET, DELAYED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20090714 |
| Marketing Category Name | NDA |
| Labeler Name | Target Corporation |
| Substance Name | OMEPRAZOLE |
| Strength Number | 20 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
