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omeprazole
omeprazole - 11822-0915-5 - (Omeprazole)
Drug Information of omeprazole
| Product NDC: | 11822-0915 |
| 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: | 11822-0915 |
| Labeler Name: | Rite Aid Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | NDA022032 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20080225 |
Package Information of omeprazole
| Package NDC: | 11822-0915-5 |
| Package Description: | 1 BOTTLE in 1 CARTON (11822-0915-5) > 14 TABLET, DELAYED RELEASE in 1 BOTTLE |
NDC Information of omeprazole
| NDC Code | 11822-0915-5 |
| Proprietary Name | omeprazole |
| Package Description | 1 BOTTLE in 1 CARTON (11822-0915-5) > 14 TABLET, DELAYED RELEASE in 1 BOTTLE |
| Product NDC | 11822-0915 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Omeprazole |
| Dosage Form Name | TABLET, DELAYED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20080225 |
| Marketing Category Name | NDA |
| Labeler Name | Rite Aid Corporation |
| Substance Name | OMEPRAZOLE |
| Strength Number | 20 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
