NDC 68382-117 – risperidone
Risperidone 4 mg/1 · Tablet, Film Coated · Oral
Product NDC68382-117
Product details
- Brand name
- risperidone
- Generic name
- risperidone
- Labeler
- Zydus Pharmaceuticals USA Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA078040
- Marketed since
- November 13, 2008
- Listing expires
- December 31, 2026
- Pharmacologic class
- Atypical Antipsychotic
Active ingredients
- Risperidone 4 mg/1
Package NDC codes (6)
| Package NDC | Description | Since |
|---|---|---|
| 68382-117-01 | 100 TABLET, FILM COATED in 1 BOTTLE (68382-117-01) | Nov 13, 2008 |
| 68382-117-05 | 500 TABLET, FILM COATED in 1 BOTTLE (68382-117-05) | Nov 13, 2008 |
| 68382-117-06 | 30 TABLET, FILM COATED in 1 BOTTLE (68382-117-06) | Nov 13, 2008 |
| 68382-117-10 | 1000 TABLET, FILM COATED in 1 BOTTLE (68382-117-10) | Nov 13, 2008 |
| 68382-117-14 | 60 TABLET, FILM COATED in 1 BOTTLE (68382-117-14) | Nov 13, 2008 |
| 68382-117-16 | 90 TABLET, FILM COATED in 1 BOTTLE (68382-117-16) | Nov 13, 2008 |
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