NDC 33342-071 – Olanzapine
Olanzapine 15 mg/1 · Tablet, Film Coated · Oral
Product NDC33342-071
Product details
- Brand name
- Olanzapine
- Generic name
- Olanzapine
- Labeler
- Macleods Pharmaceuticals Limited
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA202862
- Marketed since
- August 22, 2014
- Listing expires
- December 31, 2027
- Pharmacologic class
- Atypical Antipsychotic
Active ingredients
- Olanzapine 15 mg/1
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 33342-071-07 | 30 TABLET, FILM COATED in 1 BOTTLE (33342-071-07) | Aug 22, 2014 |
| 33342-071-11 | 100 TABLET, FILM COATED in 1 BOTTLE (33342-071-11) | Aug 22, 2014 |
| 33342-071-12 | 10 BLISTER PACK in 1 CARTON (33342-071-12) / 10 TABLET, FILM COATED in 1 BLISTER PACK | Aug 22, 2014 |
| 33342-071-15 | 500 TABLET, FILM COATED in 1 BOTTLE (33342-071-15) | Aug 22, 2014 |
| 33342-071-44 | 1000 TABLET, FILM COATED in 1 BOTTLE (33342-071-44) | Aug 22, 2014 |
Recalls mentioning this NDC
- D-0154-2025 Dec 25, 2024 · Class II
Failed Impurities/Degradation Specifications - D-0639-2022 Mar 9, 2022 · Class II
cGmp Deviations
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