Chlorpromazine Hydrochloride
- Product NDC
- 70518-0016
- 11-digit product format
- 705180016
- Labeler code
- 70518
- Product ID
- 70518-0016_f05aa84f-042e-7aa8-e053-2a95a90a4e86
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Chlorpromazine Hydrochloride
- Dosage form
- TABLET, SUGAR COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA084113
- Marketing category
- ANDA
- Marketing start
- 2016-11-25
- Marketing end
- 0000-00-00
- Substance
- CHLORPROMAZINE HYDROCHLORIDE
- Active strength
- 50 mg/1
- Pharmacologic classes
- Phenothiazine [EPC], Phenothiazines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 70518-0016-0 | 70518001600 | 30 TABLET, SUGAR COATED in 1 BLISTER PACK (70518-0016-0) | 2016-11-25 | 0000-00-00 | No | No | Current |