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LANSOPRAZOLE
LANSOPRAZOLE - 16590-890-30 - (LANSOPRAZOLE)
Drug Information of LANSOPRAZOLE
| Product NDC: | 16590-890 |
| Proprietary Name: | LANSOPRAZOLE |
| Non Proprietary Name: | LANSOPRAZOLE |
| Active Ingredient(s): | 15 mg/1 & nbsp; LANSOPRAZOLE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE, DELAYED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of LANSOPRAZOLE
| Product NDC: | 16590-890 |
| Labeler Name: | STAT Rx USA LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020406 |
| Marketing Category: | NDA AUTHORIZED GENERIC |
| Start Marketing Date: | 20091111 |
Package Information of LANSOPRAZOLE
| Package NDC: | 16590-890-30 |
| Package Description: | 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (16590-890-30) |
NDC Information of LANSOPRAZOLE
| NDC Code | 16590-890-30 |
| Proprietary Name | LANSOPRAZOLE |
| Package Description | 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (16590-890-30) |
| Product NDC | 16590-890 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | LANSOPRAZOLE |
| Dosage Form Name | CAPSULE, DELAYED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20091111 |
| Marketing Category Name | NDA AUTHORIZED GENERIC |
| Labeler Name | STAT Rx USA LLC |
| Substance Name | LANSOPRAZOLE |
| Strength Number | 15 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Proton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA] |
