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Mirtazapine
Mirtazapine - 59762-1415-3 - (Mirtazapine)
Drug Information of Mirtazapine
| Product NDC: | 59762-1415 |
| Proprietary Name: | Mirtazapine |
| Non Proprietary Name: | Mirtazapine |
| Active Ingredient(s): | 7.5 mg/1 & nbsp; Mirtazapine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Mirtazapine
| Product NDC: | 59762-1415 |
| Labeler Name: | Greenstone LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076921 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20041022 |
Package Information of Mirtazapine
| Package NDC: | 59762-1415-3 |
| Package Description: | 30 TABLET, FILM COATED in 1 BOTTLE (59762-1415-3) |
NDC Information of Mirtazapine
| NDC Code | 59762-1415-3 |
| Proprietary Name | Mirtazapine |
| Package Description | 30 TABLET, FILM COATED in 1 BOTTLE (59762-1415-3) |
| Product NDC | 59762-1415 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Mirtazapine |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20041022 |
| Marketing Category Name | ANDA |
| Labeler Name | Greenstone LLC |
| Substance Name | MIRTAZAPINE |
| Strength Number | 7.5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
