CHLORPROMAZINE HYDROCHLORIDE
- Product NDC
- 0904-6893
- 11-digit product format
- 009046893
- Labeler code
- 0904
- Product ID
- 0904-6893_1b5c3756-6012-421e-b9de-7dacd02ce698
- 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
- 0000-00-00
- Substance
- CHLORPROMAZINE HYDROCHLORIDE
- Active strength
- 25 mg/1
- Pharmacologic classes
- Phenothiazines [CS],Phenothiazine [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 0904-6893-61 | 00904689361 | 100 BLISTER PACK in 1 CARTON (0904-6893-61) > 1 TABLET, FILM COATED in 1 BLISTER PACK | 100 blister pack | 2018-09-12 | 0000-00-00 | No | No | Current |