NDC 65862-656 – Olanzapine
Olanzapine 5 mg/1 · Tablet, Orally Disintegrating · Oral
Product NDC65862-656
Product details
- Brand name
- Olanzapine
- Generic name
- Olanzapine
- Labeler
- Aurobindo Pharma Limited
- Dosage form
- Tablet, Orally Disintegrating
- Route
- Oral
- Marketing category
- ANDA · ANDA203708
- Marketed since
- May 15, 2014
- Listing expires
- December 31, 2027
- Pharmacologic class
- Atypical Antipsychotic
Active ingredients
- Olanzapine 5 mg/1
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 65862-656-03 | 3 BLISTER PACK in 1 CARTON (65862-656-03) / 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (65862-656-10) | May 15, 2014 |
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.