NDC 68788-7161 – Olanzapine
Olanzapine 5 mg/1 · Tablet, Film Coated · Oral
Product NDC68788-7161
Product details
- Brand name
- Olanzapine
- Generic name
- Olanzapine
- Labeler
- Preferred Pharmaceuticals Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA202862
- Marketed since
- June 5, 2018
- Listing expires
- December 31, 2027
- Pharmacologic class
- Atypical Antipsychotic
Active ingredients
- Olanzapine 5 mg/1
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 68788-7161-3 | 30 TABLET, FILM COATED in 1 BOTTLE (68788-7161-3) | Jun 5, 2018 |
| 68788-7161-6 | 60 TABLET, FILM COATED in 1 BOTTLE (68788-7161-6) | Jun 5, 2018 |
| 68788-7161-9 | 90 TABLET, FILM COATED in 1 BOTTLE (68788-7161-9) | Jun 5, 2018 |
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