NDC 53489-500 – Thioridazine Hydrochloride
Thioridazine Hydrochloride 100 mg/1 · Tablet, Film Coated · Oral
Product NDC53489-500
Product details
- Brand name
- Thioridazine Hydrochloride
- Generic name
- Thioridazine Hydrochloride
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA089953
- Marketed since
- October 7, 1988
- Listing expires
- December 31, 2026
- Pharmacologic class
- Phenothiazine
Active ingredients
- Thioridazine Hydrochloride 100 mg/1
Uses, dosage, side effects and warnings for Thioridazine Hydrochloride →
Package NDC codes (7)
| Package NDC | Description | Since |
|---|---|---|
| 53489-500-01 | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-500-01) | Oct 7, 1988 |
| 53489-500-02 | 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-500-02) | Oct 7, 1988 |
| 53489-500-03 | 250 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-500-03) | Oct 7, 1988 |
| 53489-500-05 | 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-500-05) | Oct 7, 1988 |
| 53489-500-06 | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-500-06) | Oct 7, 1988 |
| 53489-500-10 | 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-500-10) | Oct 7, 1988 |
| 53489-500-60 | 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-500-60) | Oct 7, 1988 |
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