Chlorpromazine Hydrochloride
- Product NDC
- 70518-2035
- 11-digit product format
- 705182035
- Labeler code
- 70518
- Product ID
- 70518-2035_899805bd-7473-f7c8-e053-2995a90a0b86
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Chlorpromazine Hydrochloride
- Dosage form
- TABLET, SUGAR COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA084114
- Marketing category
- ANDA
- Marketing start
- 2019-04-23
- Marketing end
- 0000-00-00
- Substance
- CHLORPROMAZINE HYDROCHLORIDE
- Active strength
- 100 mg/1
- Pharmacologic classes
- Phenothiazines [CS],Phenothiazine [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record