69809-0135 : Clozaril 200 mg Oral Tablet
NDC: | 69809-0135 |
Labeler: | Hls Therapeutics (Usa), Inc. |
Product Type: | Human Prescription Drug |
Drug Name: | Clozaril |
Dosage Form: | Oral Tablet |
Application #: | NDA019758 |
Rev. Date: |
Appearance:
Markings: | CLOZARIL;200;mg |
Shapes: |
Capsule |
Colors: |
Yellow |
Size (mm): | 9 |
Segments: * | 2 |
* Segments = the number of equally sized pieces which the pill can be broken into. In this case, a value of 2 indicates a scored pill which can be broken into 2 equal pieces. |
NDC Package Codes:
- 69809-0135-5: 100 TABLET IN 1 BOTTLE (69809‑0135‑5)
Active Ingredients:
- Clozapine
Dosage Strength:
- 200 mg
Inactive Ingredients:
- Silicon Dioxide
- Lactose, Unspecified Form
- Magnesium Stearate
- Povidone, Unspecified
- Starch, Corn
- Talc /
Pharmaceutical Classes:
- Atypical Antipsychotic [EPC]
Related Products:
Based on records with the same trade name.- 69809-0126 Clozaril 25 mg Oral Tablet by Hls Therapeutics (Usa), Inc.
- 69809-0127 Clozaril 100 mg Oral Tablet by Hls Therapeutics (Usa), Inc.
- 69809-0130 Clozaril 50 mg Oral Tablet by Hls Therapeutics (Usa), Inc.
- 0078-0126 Clozaril 25 mg Oral Tablet by Novartis Pharmaceuticals Corporation
- 0078-0127 Clozaril 100 mg Oral Tablet by Novartis Pharmaceuticals Corporation
- 55154-3424 Clozaril 100 mg Oral Tablet by Cardinal Health
- 64725-1260 Clozaril 25 mg Oral Tablet by Tya Pharmaceuticals
NDC QR Code
Scan the QR code below to easily reference this data in the future:< Prev: 69809-0130Next: 69811-101 >
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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.