Chlorpromazine Hydrochloride
- Product NDC
- 70518-1996
- 11-digit product format
- 705181996
- Labeler code
- 70518
- Product ID
- 70518-1996_970d880d-1640-1f03-e053-2a95a90a1c58
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Chlorpromazine Hydrochloride
- Dosage form
- TABLET, SUGAR COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA084113
- Marketing category
- ANDA
- Marketing start
- 2019-03-29
- Marketing end
- 0000-00-00
- Substance
- CHLORPROMAZINE HYDROCHLORIDE
- Active strength
- 50 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