Chlorpromazine Hydrochloride
- Product NDC
- 0615-7683
- 11-digit product format
- 006157683
- Labeler code
- 0615
- Product ID
- 0615-7683_19dd962f-55d9-47a7-8c00-e91bf0d66f5c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Chlorpromazine Hydrochloride
- Dosage form
- TABLET, SUGAR COATED
- Route
- ORAL
- Labeler
- NCS HealthCare of KY, Inc dba Vangard Labs
- Application
- ANDA084113
- Marketing category
- ANDA
- Marketing start
- 1974-07-09
- Marketing end
- 0000-00-00
- Substance
- CHLORPROMAZINE HYDROCHLORIDE
- Active strength
- 50 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#