NDC 63402-302 – Latuda
Lurasidone Hydrochloride 20 mg/1 · Tablet, Film Coated · Oral
Product NDC63402-302
Product details
- Brand name
- Latuda
- Generic name
- Lurasidone hydrochloride
- Labeler
- Sumitomo Pharma America, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- NDA · NDA200603
- Marketed since
- December 7, 2011
- Listing expires
- December 31, 2027
- Pharmacologic class
- Atypical Antipsychotic
Active ingredients
- Lurasidone Hydrochloride 20 mg/1
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 63402-302-04 | 4 BLISTER PACK in 1 CARTON (63402-302-04) / 7 TABLET, FILM COATED in 1 BLISTER PACK (63402-302-07) | Dec 7, 2011 |
| 63402-302-10 | 10 BLISTER PACK in 1 CARTON (63402-302-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK (63402-302-01) | Dec 7, 2011 |
| 63402-302-30 | 30 TABLET, FILM COATED in 1 BOTTLE (63402-302-30) | Dec 7, 2011 |
| 63402-302-50 | 500 TABLET, FILM COATED in 1 BOTTLE (63402-302-50) | Dec 7, 2011 |
| 63402-302-90 | 90 TABLET, FILM COATED in 1 BOTTLE (63402-302-90) | Dec 7, 2011 |
Other Latuda products
- 63402-304 Lurasidone Hydrochloride 40 mg/1 · Tablet, Film Coated · Sumitomo Pharma America, Inc.
- 63402-306 Lurasidone Hydrochloride 60 mg/1 · Tablet, Film Coated · Sumitomo Pharma America, Inc.
- 63402-308 Lurasidone Hydrochloride 80 mg/1 · Tablet, Film Coated · Sumitomo Pharma America, Inc.
- 63402-312 Lurasidone Hydrochloride 120 mg/1 · Tablet, Film Coated · Sumitomo Pharma America, Inc.