NDC 71335-0534 – Olanzapine
Olanzapine 5 mg/1 · Tablet, Film Coated · Oral
Product NDC71335-0534
Product details
- Brand name
- Olanzapine
- Generic name
- Olanzapine
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA202862
- Marketed since
- August 22, 2014
- Listing expires
- December 31, 2026
- Pharmacologic class
- Atypical Antipsychotic
Active ingredients
- Olanzapine 5 mg/1
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 71335-0534-1 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-0534-1) | Feb 21, 2018 |
| 71335-0534-2 | 15 TABLET, FILM COATED in 1 BOTTLE (71335-0534-2) | Dec 27, 2021 |
| 71335-0534-3 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-0534-3) | Jun 1, 2021 |
| 71335-0534-4 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-0534-4) | Dec 27, 2021 |
| 71335-0534-5 | 120 TABLET, FILM COATED in 1 BOTTLE (71335-0534-5) | Dec 27, 2021 |
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