NDC 87441-062 – Olanzapine
Olanzapine 5 mg/1 · Tablet, Film Coated · Oral
Product NDC87441-062
Product details
- Brand name
- Olanzapine
- Generic name
- Olanzapine
- Labeler
- Unit Dose Solutions, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA076255
- Marketed since
- June 29, 2026
- Listing expires
- December 31, 2027
- Pharmacologic class
- Atypical Antipsychotic
Active ingredients
- Olanzapine 5 mg/1
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 87441-062-01 | 30 TABLET, FILM COATED in 1 BLISTER PACK (87441-062-01) | Jun 29, 2026 |
Other Olanzapine products
- 68084-529 Olanzapine 20 mg/1 · Tablet, Film Coated · American Health Packaging
- 68084-740 Olanzapine 10 mg/1 · Tablet, Film Coated · American Health Packaging
- 68084-528 Olanzapine 15 mg/1 · Tablet, Film Coated · American Health Packaging
- 68084-525 Olanzapine 2.5 mg/1 · Tablet, Film Coated · American Health Packaging
- 68084-723 Olanzapine 5 mg/1 · Tablet, Film Coated · American Health Packaging
- 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.
- 60505-3111 Olanzapine 5 mg/1 · Tablet, Film Coated · Apotex Corp.
- 60505-3112 Olanzapine 7.5 mg/1 · Tablet, Film Coated · Apotex Corp.
- 60505-3114 Olanzapine 15 mg/1 · Tablet, Film Coated · Apotex Corp.
- 60505-3113 Olanzapine 10 mg/1 · Tablet, Film Coated · Apotex Corp.
- 60505-3110 Olanzapine 2.5 mg/1 · Tablet, Film Coated · Apotex Corp.