NDC 70518-1635 – Olanzapine
Olanzapine 10 mg/1 · Tablet, Film Coated · Oral
Product NDC70518-1635
Product details
- Brand name
- Olanzapine
- Generic name
- Olanzapine
- Labeler
- REMEDYREPACK INC.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA076255
- Marketed since
- November 6, 2018
- Listing expires
- December 31, 2027
- Pharmacologic class
- Atypical Antipsychotic
Active ingredients
- Olanzapine 10 mg/1
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 70518-1635-0 | 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1635-0) | Nov 6, 2018 |
| 70518-1635-1 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1635-1) | Dec 6, 2022 |
| 70518-1635-2 | 60 TABLET, FILM COATED in 1 BLISTER PACK (70518-1635-2) | Sep 21, 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.