PROCHLORPERAZINE MALEATE
- Product NDC
- 51655-096
- 11-digit product format
- 516550096
- Labeler code
- 51655
- Product ID
- 51655-096_4ab90401-073e-37f9-e063-6294a90a93f1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prochlorperazine Maleate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Northwind Health Company, LLC
- Application
- ANDA040268
- Marketing category
- ANDA
- Marketing start
- 2014-04-28
- Substance
- PROCHLORPERAZINE MALEATE
- Active strength
- 5 mg/1
- Pharmacologic classes
- Phenothiazine [EPC], Phenothiazines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- PROCHLORPERAZINE MALEATE
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| PROCHLORPERAZINE MALEATE | 5 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | I1T8O1JTL6 |
| Rxcui | 312635 |
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 51655-096-87 | PROCHLORPERAZINE MALEATE | 6 in 1 BOTTLE | TABLET | 6 | | 5 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51655-096 | PROCHLORPERAZINE MALEATE TABLET [NORTHWIND PHARMACEUTICALS, LLC] | 2 | Current NDC, Legacy NDC, 1 package rows | 20240725_c524a28e-1e08-4aa6-a9f0-0a3280a3c213.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 51655-096-87 | 51655009687 | 6 TABLET in 1 BOTTLE (51655-096-87) | 6 tablet | 2014-04-28 | No | No | Historical |