50090-1730 : Olanzapine 10 mg Oral Tablet


NDC50090-1730
Labeler: A-s Medication Solutions
Product Type: Human Prescription Drug
Drug Name:  Olanzapine
Dosage Form: Oral Tablet
Application #: ANDA091038
Rev. Date: 


Appearance:


Markings: 554
Shapes:  Oval
Colors:  Yellow
Size (mm): 12
Segments: * 1

* Segments = the number of equally sized pieces which the pill can be broken into. In this case, a value of 1 indicates a solid pill with no score lines.

NDC Package Codes:

  • 50090-1730-0: 14 TABLET IN 1 BOTTLE (50090‑1730‑0)

Active Ingredients:

  • Olanzapine

Dosage Strength:

  • 10 mg

Inactive Ingredients:

  • Anhydrous Lactose
  • Cellulose, Microcrystalline
  • Crospovidone
  • Hydroxypropyl Cellulose, Low Substituted
  • Magnesium Stearate
  • Silicon Dioxide

Pharmaceutical Classes:

  • Atypical Antipsychotic [EPC]

Related Products:

Based on records with the same trade name.
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  • 50090-3100 Olanzapine 10 mg Oral Tablet, Film Coated by A-s Medication Solutions
  • 50090-3267 Olanzapine 10 mg Oral Tablet, Film Coated by A-s Medication Solutions
  • 50090-3405 Olanzapine 10 mg Oral Tablet, Orally Disintegrating by A-s Medication Solutions
  • 50090-3933 Olanzapine 10 mg Oral Tablet by A-s Medication Solutions
  • 50090-3934 Olanzapine 10 mg Oral Tablet by A-s Medication Solutions
  • 50090-3958 Olanzapine 10 mg Oral Tablet, Orally Disintegrating by A-s Medication Solutions
  • 50090-3967 Olanzapine 5 mg Oral Tablet, Orally Disintegrating by A-s Medication Solutions
  • 50090-4040 Olanzapine 5 mg Oral Tablet by A-s Medication Solutions
  • 50090-5047 Olanzapine 10 mg Oral Tablet, Film Coated by A-s Medication Solutions
  • 50090-5102 Olanzapine 5 mg Oral Tablet, Film Coated by A-s Medication Solutions
  • 50090-6111 Olanzapine 10 mg Oral Tablet, Orally Disintegrating by A-s Medication Solutions
  • 0093-5105 Olanzapine 20 mg Oral Tablet by Teva Pharmaceuticals USA
  • 0093-5245 Olanzapine 5 mg Disintegrating Tablet by Teva Pharmaceuticals USA 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.