Chlorpromazine Hydrochloride
- Product NDC
- 51079-517
- 11-digit product format
- 510790517
- Labeler code
- 51079
- Product ID
- 51079-517_9a252b62-8427-382e-e053-2995a90a3222
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Chlorpromazine Hydrochloride
- Dosage form
- TABLET, SUGAR COATED
- Route
- ORAL
- Labeler
- Mylan Institutional Inc.
- Application
- ANDA084115
- Marketing category
- ANDA
- Marketing start
- 1994-11-28
- Marketing end
- 2021-04-30
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 51079-517-20 | 51079051720 | 100 BLISTER PACK in 1 CARTON (51079-517-20) > 1 TABLET, SUGAR COATED in 1 BLISTER PACK (51079-517-01) | 100 blister pack | 1994-11-28 | 2021-04-30 | No | No | Current |