CHLORPROMAZINE HYDROCHLORIDE
- Product NDC
- 0904-6894
- 11-digit product format
- 009046894
- Labeler code
- 0904
- Product ID
- 0904-6894_f0711d3f-c13e-4d83-b92d-1045c1e9cce1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- CHLORPROMAZINE HYDROCHLORIDE
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Major Pharmaceuticals
- Application
- ANDA209755
- Marketing category
- ANDA
- Marketing start
- 2018-09-12
- Marketing end
- 2022-08-31
- Substance
- CHLORPROMAZINE HYDROCHLORIDE
- Active strength
- 50 mg/1
- Pharmacologic classes
- Phenothiazine [EPC], Phenothiazines [CS]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0904-6894-61 | 00904689461 | 100 BLISTER PACK in 1 CARTON (0904-6894-61) > 1 TABLET, FILM COATED in 1 BLISTER PACK | 100 blister pack | 2018-09-12 | 0000-00-00 | No | No | Current |