NDC 72789-341 – Olanzapine
Olanzapine 20 mg/1 · Tablet, Film Coated · Oral
Product NDC72789-341
Product details
- Brand name
- Olanzapine
- Generic name
- Olanzapine
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA202862
- Marketed since
- August 22, 2014
- Listing expires
- December 31, 2027
- Pharmacologic class
- Atypical Antipsychotic
Active ingredients
- Olanzapine 20 mg/1
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 72789-341-90 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-341-90) | Aug 1, 2023 |
Other Olanzapine products
- 68084-525 Olanzapine 2.5 mg/1 · Tablet, Film Coated · American Health Packaging
- 68084-528 Olanzapine 15 mg/1 · Tablet, Film Coated · American Health Packaging
- 68084-740 Olanzapine 10 mg/1 · Tablet, Film Coated · American Health Packaging
- 68084-723 Olanzapine 5 mg/1 · Tablet, Film Coated · American Health Packaging
- 68084-529 Olanzapine 20 mg/1 · Tablet, Film Coated · American Health Packaging
- 0517-0955 Olanzapine 10 mg/2mL · Injection, Powder, Lyophilized, For Solution · American Regent, Inc.
- 83854-003 Olanzapine 10 mg/2mL · Injection, Powder, Lyophilized, For Solution · Anthea Pharma Private Limited
- 71610-419 Olanzapine 15 mg/1 · Tablet, Film Coated · Aphena Pharma Solutions - Tennessee, LLC
- 60505-3140 Olanzapine 20 mg/1 · Tablet, Film Coated · Apotex Corp.
- 60505-3278 Olanzapine 20 mg/1 · Tablet, Orally Disintegrating · Apotex Corp.
- 60505-3110 Olanzapine 2.5 mg/1 · Tablet, Film Coated · Apotex Corp.
- 60505-3113 Olanzapine 10 mg/1 · Tablet, Film Coated · Apotex Corp.