Prochlorperazine Maleate
- Product NDC
- 70710-1667
- 11-digit product format
- 707101667
- Labeler code
- 70710
- Product ID
- 70710-1667_da187256-50af-400b-ab27-a073f3fbe81a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prochlorperazine Maleate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Zydus Pharmaceuticals (USA) Inc.
- Application
- ANDA216495
- Marketing category
- ANDA
- Marketing start
- 2022-08-10
- Substance
- PROCHLORPERAZINE MALEATE
- Active strength
- 5 mg/1
- Pharmacologic classes
- Phenothiazine [EPC], Phenothiazines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Prochlorperazine Maleate
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| PROCHLORPERAZINE MALEATE | 5 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | I1T8O1JTL6 |
| Rxcui | 198365, 312635 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70710-1667-1 | Prochlorperazine Maleate | 100 in 1 BOTTLE | TABLET | 100 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70710-1667 | PROCHLORPERAZINE MALEATE TABLET [ZYDUS PHARMACEUTICALS (USA) INC.] | 6 | Current NDC, Legacy NDC, 1 package rows | 20241207_d4a34138-a01b-418f-8e0f-e81f6e1cfd89.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 |
|---|
| 70710-1667-1 | 70710166701 | 100 TABLET in 1 BOTTLE (70710-1667-1) | 100 tablet | 2022-08-10 | 0000-00-00 | No | No | Current |