NDC 0832-6021 – Chlorpromazine Hydrochloride
Chlorpromazine Hydrochloride 200 mg/1 · Tablet, Film Coated · Oral
Product NDC0832-6021
Product details
- Brand name
- Chlorpromazine Hydrochloride
- Generic name
- Chlorpromazine Hydrochloride
- Labeler
- Upsher-Smith Laboratories, LLC
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA084115
- Marketed since
- August 3, 2011
- Listing expires
- December 31, 2027
- Pharmacologic class
- Phenothiazine
Active ingredients
- Chlorpromazine Hydrochloride 200 mg/1
Uses, dosage, side effects and warnings for Chlorpromazine Hydrochloride →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 0832-6021-00 | 100 TABLET, FILM COATED in 1 BOTTLE (0832-6021-00) | Aug 6, 2021 |
| 0832-6021-01 | 1 BLISTER PACK in 1 CARTON (0832-6021-01) / 100 TABLET, FILM COATED in 1 BLISTER PACK (0832-6021-89) | Aug 6, 2021 |
| 0832-6021-10 | 1000 TABLET, FILM COATED in 1 BOTTLE (0832-6021-10) | Aug 6, 2021 |
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