Chlorpromazine Hydrochloride
- Product NDC
- 51079-516
- 11-digit product format
- 510790516
- Labeler code
- 51079
- Product ID
- 51079-516_9a252b62-8427-382e-e053-2995a90a3222
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Chlorpromazine Hydrochloride
- Dosage form
- TABLET, SUGAR COATED
- Route
- ORAL
- Labeler
- Mylan Institutional Inc.
- Application
- ANDA084114
- Marketing category
- ANDA
- Marketing start
- 1994-11-28
- Marketing end
- 2020-08-31
- Substance
- CHLORPROMAZINE HYDROCHLORIDE
- Active strength
- 100 mg/1
- Pharmacologic classes
- Phenothiazines [CS],Phenothiazine [EPC]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record