Chlorpromazine Hydrochloride
- Product NDC
- 70518-3086
- 11-digit product format
- 705183086
- Labeler code
- 70518
- Product ID
- 70518-3086_c1aa231e-2922-46e3-e053-2995a90ad370
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Chlorpromazine Hydrochloride
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA212996
- Marketing category
- ANDA
- Marketing start
- 2021-05-06
- 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
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70518-3086 | CHLORPROMAZINE HYDROCHLORIDE TABLET, COATED [REMEDYREPACK INC.] | 4 | Legacy NDC | 20240420_9d41121b-0036-47a1-ad39-5814996f8277.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-3086-0 | 70518308600 | 30 TABLET, COATED in 1 BLISTER PACK (70518-3086-0) | 2021-05-06 | 0000-00-00 | No | No | Current |