0781-3159 : Olanzapine 10 mg/2ml Intramuscular Injection, Powder, for Solution
NDC: | 0781-3159 |
Labeler: | Sandoz Inc |
Product Type: | Human Prescription Drug |
Drug Name: | Olanzapine |
Dosage Form: | Intramuscular Injection, Powder, for Solution |
Application #: | ANDA201588 |
Rev. Date: |
NDC Package Codes:
- 0781-3159-72: 1 VIAL IN 1 CARTON (0781‑3159‑72) > 2 ML IN 1 VIAL
Active Ingredients:
- Olanzapine
Dosage Strength:
- 10 mg/2mL
Pharmaceutical Classes:
- Atypical Antipsychotic [EPC]
Related Products:
Based on records with the same trade name.- 0781-9105 Olanzapine 10 mg/2ml Intramuscular Injection, Powder, for Solution by Sandoz Inc
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- 0093-5246 Olanzapine 10 mg Disintegrating Tablet by Teva Pharmaceuticals USA Inc
- 0093-5247 Olanzapine 15 mg Disintegrating Tablet by Teva Pharmaceuticals USA Inc
- 0093-5248 Olanzapine 20 mg Disintegrating Tablet by Teva Pharmaceuticals USA Inc
- 0093-5767 Olanzapine 2.5 mg Oral Tablet by Teva Pharmaceuticals USA Inc
- 0093-5768 Olanzapine 5 mg Oral Tablet by Teva Pharmaceuticals USA Inc
- 0093-5769 Olanzapine 7.5 mg Oral Tablet by Teva Pharmaceuticals USA Inc
- 0093-5770 Olanzapine 10 mg Oral Tablet by Teva Pharmaceuticals USA Inc
- 0093-5771 Olanzapine 15 mg Oral Tablet by Teva Pharmaceuticals USA Inc
- 0378-5157 Olanzapine 2.5 mg Oral Tablet by Mylan Pharmaceuticals Inc.
- 0378-5212 Olanzapine 5 mg Oral Tablet by Mylan Pharmaceuticals Inc.
- 0378-5335 Olanzapine 7.5 mg Oral Tablet by Mylan Pharmaceuticals Inc.
- 0378-5454 Olanzapine 10 mg Oral Tablet by Mylan Pharmaceuticals Inc.
- 0378-5510 Olanzapine 5 mg Oral Tablet, Orally Disintegrating by Mylan Pharmaceuticals Inc.
- 0378-5511 Olanzapine 10 mg Oral Tablet, Orally Disintegrating by Mylan Pharmaceuticals Inc.
- 0378-5512 Olanzapine 15 mg Oral Tablet, Orally Disintegrating by Mylan Pharmaceuticals Inc.
- 0378-5513 Olanzapine 20 mg Oral Tablet, Orally Disintegrating by Mylan Pharmaceuticals Inc.
- 0378-5522 Olanzapine 15 mg Oral Tablet by Mylan Pharmaceuticals Inc.
- More related products ...
NDC QR Code
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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.