Chlorpromazine
- Product NDC
- 51862-590
- 11-digit product format
- 518620590
- Labeler code
- 51862
- Product ID
- 51862-590_8f0da323-7674-441c-bfcb-66bd8807345d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Chlorpromazine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Mayne Pharma Inc.
- Application
- ANDA213590
- Marketing category
- ANDA
- Marketing start
- 2021-07-15
- Marketing end
- 0000-00-00
- Substance
- CHLORPROMAZINE HYDROCHLORIDE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Phenothiazines [CS],Phenothiazine [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 51862-590-01 | 51862059001 | 100 TABLET in 1 BOTTLE (51862-590-01) | 100 tablet | 2021-07-15 | 0000-00-00 | No | No | Current |