Chlorpromazine
- Product NDC
- 0615-1546
- 11-digit product format
- 006151546
- Labeler code
- 0615
- Product ID
- 0615-1546_4d95826c-dfb7-4752-86ea-54f4b83e04aa
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Chlorpromazine Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- NCS HealthCare of KY, Inc dba Vangard Labs
- Application
- ANDA080439
- Marketing category
- ANDA
- Marketing start
- 1973-01-03
- Marketing end
- 0000-00-00
- Substance
- CHLORPROMAZINE HYDROCHLORIDE
- Active strength
- 25 mg/1
- Pharmacologic classes
- Phenothiazines [CS],Phenothiazine [EPC]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#