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OMESEC
OMESEC - 16853-1308-1 - (Omeprazole)
Drug Information of OMESEC
| Product NDC: | 16853-1308 |
| Proprietary Name: | OMESEC |
| 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 OMESEC
| Product NDC: | 16853-1308 |
| Labeler Name: | Corporacion Infarmasa |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA075410 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100228 |
Package Information of OMESEC
| Package NDC: | 16853-1308-1 |
| Package Description: | 14 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (16853-1308-1) |
NDC Information of OMESEC
| NDC Code | 16853-1308-1 |
| Proprietary Name | OMESEC |
| Package Description | 14 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (16853-1308-1) |
| Product NDC | 16853-1308 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Omeprazole |
| Dosage Form Name | CAPSULE, DELAYED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20100228 |
| Marketing Category Name | ANDA |
| Labeler Name | Corporacion Infarmasa |
| Substance Name | OMEPRAZOLE |
| Strength Number | 20 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
