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Zegerid OTC
Zegerid OTC - 11523-7265-3 - (Omeprazole and Sodium Bicarbonate)
Drug Information of Zegerid OTC
| Product NDC: | 11523-7265 |
| Proprietary Name: | Zegerid OTC |
| Non Proprietary Name: | Omeprazole and Sodium Bicarbonate |
| Active Ingredient(s): | 20; 1100 mg/1; mg/1 & nbsp; Omeprazole and Sodium Bicarbonate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Zegerid OTC
| Product NDC: | 11523-7265 |
| Labeler Name: | MSD Consumer Care, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | NDA022281 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20100401 |
Package Information of Zegerid OTC
| Package NDC: | 11523-7265-3 |
| Package Description: | 3 BOTTLE in 1 CARTON (11523-7265-3) > 14 CAPSULE in 1 BOTTLE |
NDC Information of Zegerid OTC
| NDC Code | 11523-7265-3 |
| Proprietary Name | Zegerid OTC |
| Package Description | 3 BOTTLE in 1 CARTON (11523-7265-3) > 14 CAPSULE in 1 BOTTLE |
| Product NDC | 11523-7265 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Omeprazole and Sodium Bicarbonate |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20100401 |
| Marketing Category Name | NDA |
| Labeler Name | MSD Consumer Care, Inc. |
| Substance Name | OMEPRAZOLE; SODIUM BICARBONATE |
| Strength Number | 20; 1100 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |
