NDC 43598-165 – Olanzapine
Olanzapine 7.5 mg/1 · Tablet, Film Coated · Oral
Product NDC43598-165
Product details
- Brand name
- Olanzapine
- Generic name
- Olanzapine
- Labeler
- Dr. Reddy's Laboratories Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA076255
- Marketed since
- December 10, 2013
- Listing expires
- December 31, 2027
- Pharmacologic class
- Atypical Antipsychotic
Active ingredients
- Olanzapine 7.5 mg/1
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 43598-165-01 | 100 TABLET, FILM COATED in 1 BOTTLE (43598-165-01) | Dec 10, 2013 |
| 43598-165-05 | 500 TABLET, FILM COATED in 1 BOTTLE (43598-165-05) | Dec 10, 2013 |
| 43598-165-30 | 30 TABLET, FILM COATED in 1 BOTTLE (43598-165-30) | Dec 10, 2013 |
| 43598-165-60 | 60 TABLET, FILM COATED in 1 BOTTLE (43598-165-60) | Dec 10, 2013 |
| 43598-165-78 | 10 BLISTER PACK in 1 CARTON (43598-165-78) / 10 TABLET, FILM COATED in 1 BLISTER PACK (43598-165-79) | Dec 10, 2013 |
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