Chlorpromazine hydrochloride
- Product NDC
- 70518-3034
- 11-digit product format
- 705183034
- Labeler code
- 70518
- Product ID
- 70518-3034_bc803539-69c2-dd55-e053-2a95a90ab55c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Chlorpromazine hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA213368
- Marketing category
- ANDA
- Marketing start
- 2021-03-01
- 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#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-3034-0 | 70518303400 | 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3034-0) | 2021-03-01 | 0000-00-00 | No | No | Current |