Chlorpromazine Hydrochloride
- Product NDC
- 0781-5917
- 11-digit product format
- 007815917
- Labeler code
- 0781
- Product ID
- 0781-5917_78f4040a-9630-4f29-a2b4-6fc3cbd3b482
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Chlorpromazine Hydrochloride
- Dosage form
- TABLET, SUGAR COATED
- Route
- ORAL
- Labeler
- Sandoz Inc
- Application
- ANDA084115
- Marketing category
- ANDA
- Marketing start
- 1974-07-09
- Marketing end
- 2022-08-31
- Substance
- CHLORPROMAZINE HYDROCHLORIDE
- Active strength
- 200 mg/1
- Pharmacologic classes
- Phenothiazines [CS],Phenothiazine [EPC]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 0781-5917-01 | 00781591701 | 100 TABLET, SUGAR COATED in 1 BOTTLE (0781-5917-01) | 2017-01-13 | 2022-08-31 | No | No | Current |