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Olanzapine
Olanzapine - 0093-5771-01 - (Olanzapine)
Drug Information of Olanzapine
| Product NDC: | 0093-5771 |
| Proprietary Name: | Olanzapine |
| Non Proprietary Name: | Olanzapine |
| Active Ingredient(s): | 15 mg/1 & nbsp; Olanzapine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Olanzapine
| Product NDC: | 0093-5771 |
| Labeler Name: | Teva Pharmaceuticals USA Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076000 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20111024 |
Package Information of Olanzapine
| Package NDC: | 0093-5771-01 |
| Package Description: | 100 TABLET, FILM COATED in 1 BOTTLE (0093-5771-01) |
NDC Information of Olanzapine
| NDC Code | 0093-5771-01 |
| Proprietary Name | Olanzapine |
| Package Description | 100 TABLET, FILM COATED in 1 BOTTLE (0093-5771-01) |
| Product NDC | 0093-5771 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Olanzapine |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20111024 |
| Marketing Category Name | ANDA |
| Labeler Name | Teva Pharmaceuticals USA Inc |
| Substance Name | OLANZAPINE |
| Strength Number | 15 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Atypical Antipsychotic [EPC] |
