PROCHLORPERAZINE MALEATE
- Product NDC
- 70934-419
- 11-digit product format
- 709340419
- Labeler code
- 70934
- Product ID
- 70934-419_af702bf9-0bf4-312f-e053-2995a90acb2e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prochlorperazine maleate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. DBA Northwind Pharmaceuticals
- Application
- ANDA040268
- Marketing category
- ANDA
- Marketing start
- 2019-08-02
- Marketing end
- 0000-00-00
- Substance
- PROCHLORPERAZINE MALEATE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Phenothiazine [EPC],Phenothiazines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70934-419-06 | 70934041906 | 6 TABLET in 1 BOTTLE, PLASTIC (70934-419-06) | 6 tablet | 2019-08-02 | 0000-00-00 | No | No | Current |