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Lansoprazole
Lansoprazole - 64679-669-06 - (Lansoprazole)
Drug Information of Lansoprazole
| Product NDC: | 64679-669 |
| 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: | 64679-669 |
| Labeler Name: | Wockhardt USA LLC. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA202176 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120810 |
Package Information of Lansoprazole
| Package NDC: | 64679-669-06 |
| Package Description: | 10 BLISTER PACK in 1 CARTON (64679-669-06) > 10 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK |
NDC Information of Lansoprazole
| NDC Code | 64679-669-06 |
| Proprietary Name | Lansoprazole |
| Package Description | 10 BLISTER PACK in 1 CARTON (64679-669-06) > 10 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK |
| Product NDC | 64679-669 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Lansoprazole |
| Dosage Form Name | CAPSULE, DELAYED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20120810 |
| Marketing Category Name | ANDA |
| Labeler Name | Wockhardt USA LLC. |
| Substance Name | LANSOPRAZOLE |
| Strength Number | 15 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Proton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA] |
