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LOXITANE
LOXITANE - 52544-494-10 - (loxapine succinate)
Drug Information of LOXITANE
| Product NDC: | 52544-494 |
| Proprietary Name: | LOXITANE |
| Non Proprietary Name: | loxapine succinate |
| Active Ingredient(s): | 5 mg/1 & nbsp; loxapine succinate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of LOXITANE
| Product NDC: | 52544-494 |
| Labeler Name: | Watson Pharma, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA072204 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19880615 |
Package Information of LOXITANE
| Package NDC: | 52544-494-10 |
| Package Description: | 1000 CAPSULE in 1 BOTTLE, PLASTIC (52544-494-10) |
NDC Information of LOXITANE
| NDC Code | 52544-494-10 |
| Proprietary Name | LOXITANE |
| Package Description | 1000 CAPSULE in 1 BOTTLE, PLASTIC (52544-494-10) |
| Product NDC | 52544-494 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | loxapine succinate |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 19880615 |
| Marketing Category Name | ANDA |
| Labeler Name | Watson Pharma, Inc. |
| Substance Name | LOXAPINE SUCCINATE |
| Strength Number | 5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
