Chlorpromazine Hydrochloride
- Product NDC
- 70518-1608
- 11-digit product format
- 705181608
- Labeler code
- 70518
- Product ID
- 70518-1608_c340b4c5-5942-0c31-e053-2995a90a2f3a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Chlorpromazine Hydrochloride
- Dosage form
- TABLET, SUGAR COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA084112
- Marketing category
- ANDA
- Marketing start
- 2018-10-29
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-1608-0 | 70518160800 | 30 TABLET, SUGAR COATED in 1 BLISTER PACK (70518-1608-0) | 2018-10-29 | 0000-00-00 | No | No | Current |