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Omeprazole
Omeprazole - 52959-722-15 - (Omeprazole)
Drug Information of Omeprazole
| Product NDC: | 52959-722 |
| Proprietary Name: | Omeprazole |
| Non Proprietary Name: | Omeprazole |
| Active Ingredient(s): | 20 mg/1 & nbsp; Omeprazole |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE, DELAYED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Omeprazole
| Product NDC: | 52959-722 |
| Labeler Name: | H.J. Harkins Company, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075876 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110114 |
Package Information of Omeprazole
| Package NDC: | 52959-722-15 |
| Package Description: | 15 CAPSULE, DELAYED RELEASE in 1 BOTTLE (52959-722-15) |
NDC Information of Omeprazole
| NDC Code | 52959-722-15 |
| Proprietary Name | Omeprazole |
| Package Description | 15 CAPSULE, DELAYED RELEASE in 1 BOTTLE (52959-722-15) |
| Product NDC | 52959-722 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Omeprazole |
| Dosage Form Name | CAPSULE, DELAYED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20110114 |
| Marketing Category Name | ANDA |
| Labeler Name | H.J. Harkins Company, Inc. |
| Substance Name | OMEPRAZOLE |
| Strength Number | 20 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Proton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA] |
