NDC 55111-168 – Olanzapine
Olanzapine 20 mg/1 · Tablet, Film Coated · Oral
Product NDC55111-168
Product details
- Brand name
- Olanzapine
- Generic name
- Olanzapine
- Labeler
- Dr. Reddy's Laboratories Ltd.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA076133
- Marketed since
- April 23, 2012
- Listing expires
- December 31, 2027
- Pharmacologic class
- Atypical Antipsychotic
Active ingredients
- Olanzapine 20 mg/1
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 55111-168-01 | 100 TABLET, FILM COATED in 1 BOTTLE (55111-168-01) | Apr 23, 2012 |
| 55111-168-05 | 500 TABLET, FILM COATED in 1 BOTTLE (55111-168-05) | Apr 23, 2012 |
| 55111-168-30 | 30 TABLET, FILM COATED in 1 BOTTLE (55111-168-30) | Apr 23, 2012 |
| 55111-168-60 | 60 TABLET, FILM COATED in 1 BOTTLE (55111-168-60) | Apr 23, 2012 |
| 55111-168-78 | 10 BLISTER PACK in 1 CARTON (55111-168-78) / 10 TABLET, FILM COATED in 1 BLISTER PACK (55111-168-79) | Apr 23, 2012 |
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