PROCHLORPERAZINE MALEATE
- Product NDC
- 70518-1620
- 11-digit product format
- 705181620
- Labeler code
- 70518
- Product ID
- 70518-1620_501f938b-ec64-d867-e063-6394a90aa760
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prochlorperazine maleate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA040268
- Marketing category
- ANDA
- Marketing start
- 2018-10-31
- 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 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70518-1620-0 | PROCHLORPERAZINE MALEATE | 30 in 1 BLISTER PACK | TABLET | 30 | | 10 |
| 70518-1620-1 | PROCHLORPERAZINE MALEATE | 50 in 1 BOX | TABLET | 50 | | 10 |
| 70518-1620-2 | PROCHLORPERAZINE MALEATE | 1 in 1 POUCH | TABLET | 1 | | 10 |
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 |
|---|
| 70518-1620-0 | 70518162000 | 30 TABLET in 1 BLISTER PACK (70518-1620-0) | 30 tablet | 2018-10-31 | 0000-00-00 | No | No | Current |
| 70518-1620-1 | 70518162001 | 50 POUCH in 1 BOX (70518-1620-1) / 1 TABLET in 1 POUCH (70518-1620-2) | 50 pouch | 2026-04-22 | | No | No | Historical |
| 70518-1620-2 | 70518162002 | 1 in 1 POUCH | | | | | | Historical |