NDC 71335-0714 – Olanzapine
Olanzapine 5 mg/1 · Tablet, Film Coated · Oral
Product NDC71335-0714
Product details
- Brand name
- Olanzapine
- Generic name
- Olanzapine
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA076255
- Marketed since
- December 10, 2013
- Listing expires
- December 31, 2026
- Pharmacologic class
- Atypical Antipsychotic
Active ingredients
- Olanzapine 5 mg/1
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 71335-0714-1 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-0714-1) | Mar 2, 2018 |
| 71335-0714-2 | 15 TABLET, FILM COATED in 1 BOTTLE (71335-0714-2) | Dec 27, 2021 |
| 71335-0714-3 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-0714-3) | Dec 27, 2021 |
| 71335-0714-4 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-0714-4) | Dec 27, 2021 |
| 71335-0714-5 | 120 TABLET, FILM COATED in 1 BOTTLE (71335-0714-5) | Dec 27, 2021 |
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