PROCHLORPERAZINE MALEATE
- Product NDC
- 50090-2839
- 11-digit product format
- 500902839
- Labeler code
- 50090
- Product ID
- 50090-2839_9d245806-9096-4ca2-aa26-574e7f3e9acb
- 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
- Substance
- PROCHLORPERAZINE MALEATE
- Active strength
- 10 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 | 10 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | I1T8O1JTL6 |
| Rxcui | 198365, 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 |
|---|
| 50090-2839-0 | PROCHLORPERAZINE MALEATE | 30 in 1 BOTTLE | TABLET | 30 | | 18 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-2839 | PROCHLORPERAZINE MALEATE TABLET PROCHLORPERAZINE MALEATE TABLET [A-S MEDICATION SOLUTIONS] | 16 | Current NDC, Legacy NDC, 1 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 |
|---|
| 50090-2839-0 | 50090283900 | 30 TABLET in 1 BOTTLE (50090-2839-0) | 30 tablet | 2017-02-03 | 0000-00-00 | No | No | Current |