Chlorpromazine Hydrochloride
- Product NDC
- 0832-0300
- 11-digit product format
- 008320300
- Labeler code
- 0832
- Product ID
- 0832-0300_887ebd0c-9fef-47b4-8096-20f67e1de49f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Chlorpromazine Hydrochloride
- Dosage form
- TABLET, SUGAR COATED
- Route
- ORAL
- Labeler
- Upsher-Smith Laboratories, Inc.
- Application
- ANDA083386
- Marketing category
- ANDA
- Marketing start
- 2011-08-08
- Marketing end
- 0000-00-00
- Substance
- CHLORPROMAZINE HYDROCHLORIDE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Phenothiazine [EPC], Phenothiazines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0832-0300-00 | 00832030000 | 100 TABLET, SUGAR COATED in 1 BOTTLE (0832-0300-00) | 2011-08-08 | 0000-00-00 | No | No | Current |
| 0832-0300-10 | 00832030010 | 1000 TABLET, SUGAR COATED in 1 BOTTLE (0832-0300-10) | 2011-08-08 | 0000-00-00 | No | No | Current |