PROCHLORPERAZINE MALEATE
- Product NDC
- 67296-2195
- 11-digit product format
- 672962195
- Labeler code
- 67296
- Product ID
- 67296-2195_4727abc5-0f6a-867f-e063-6294a90ae8ae
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prochlorperazine Maleate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Redpharm Drug
- Application
- ANDA217478
- Marketing category
- ANDA
- Marketing start
- 2025-01-31
- Substance
- PROCHLORPERAZINE MALEATE
- Active strength
- 10 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 | 10 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | I1T8O1JTL6 |
| Rxcui | 198365 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 67296-2195-1 | PROCHLORPERAZINE MALEATE | 100 in 1 BOTTLE | TABLET | 100 | | 2 |
| 67296-2195-2 | PROCHLORPERAZINE MALEATE | 15 in 1 BOTTLE | TABLET | 15 | | 2 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 67296-2195-1 | 67296219501 | 100 TABLET in 1 BOTTLE (67296-2195-1) | 100 tablet | 2025-01-31 | No | No | Current |
| 67296-2195-2 | 67296219502 | 15 TABLET in 1 BOTTLE (67296-2195-2) | 15 tablet | 2025-01-31 | No | No | Current |