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omeprazole
omeprazole - 37808-915-55 - (Omeprazole)
Drug Information of omeprazole
| Product NDC: | 37808-915 |
| Proprietary Name: | 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 omeprazole
| Product NDC: | 37808-915 |
| Labeler Name: | H E B |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | NDA022032 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20080229 |
Package Information of omeprazole
| Package NDC: | 37808-915-55 |
| Package Description: | 3 CARTON in 1 CARTON (37808-915-55) > 1 BLISTER PACK in 1 CARTON > 14 TABLET, DELAYED RELEASE in 1 BLISTER PACK |
NDC Information of omeprazole
| NDC Code | 37808-915-55 |
| Proprietary Name | omeprazole |
| Package Description | 3 CARTON in 1 CARTON (37808-915-55) > 1 BLISTER PACK in 1 CARTON > 14 TABLET, DELAYED RELEASE in 1 BLISTER PACK |
| Product NDC | 37808-915 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Omeprazole |
| Dosage Form Name | TABLET, DELAYED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20080229 |
| Marketing Category Name | NDA |
| Labeler Name | H E B |
| Substance Name | OMEPRAZOLE |
| Strength Number | 20 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
