PROCHLORPERAZINE MALEATE
- Product NDC
- 50090-2241
- 11-digit product format
- 500902241
- Labeler code
- 50090
- Product ID
- 50090-2241_a605f947-409e-4835-941a-d841f4e9dc8e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prochlorperazine Maleate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA040268
- Marketing category
- ANDA
- Marketing start
- 1998-03-01
- Marketing end
- 0000-00-00
- Substance
- PROCHLORPERAZINE MALEATE
- Active strength
- 5 mg/1
- Pharmacologic classes
- Phenothiazine [EPC],Phenothiazines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
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 |
|---|
| 50090-2241-0 | PROCHLORPERAZINE MALEATE | 3 in 1 BOTTLE | TABLET | 3 | | 18 |
| 50090-2241-5 | PROCHLORPERAZINE MALEATE | 6 in 1 BOTTLE | TABLET | 6 | | 18 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-2241 | PROCHLORPERAZINE MALEATE TABLET PROCHLORPERAZINE MALEATE TABLET [A-S MEDICATION SOLUTIONS] | 16 | Legacy NDC, 2 package rows | 20240201_8b58b63c-0a75-406b-bb29-acf0a40353bd.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-2241-0 | 50090224100 | 3 TABLET in 1 BOTTLE (50090-2241-0) | 3 tablet | 2018-10-11 | 0000-00-00 | No | No | Current |
| 50090-2241-5 | 50090224105 | 6 TABLET in 1 BOTTLE (50090-2241-5) | 6 tablet | 2015-11-24 | 0000-00-00 | No | No | Current |