PROCHLORPERAZINE MALEATE
- Product NDC
- 72162-2262
- 11-digit product format
- 721622262
- Labeler code
- 72162
- Product ID
- 72162-2262_99b1f190-48d4-4f50-9ca3-8cda21fd37f0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prochlorperazine maleate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- 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 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72162-2262-1 | PROCHLORPERAZINE MALEATE | 100 in 1 BOTTLE | TABLET | 100 | | 102 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72162-2262 | PROCHLORPERAZINE MALEATE (PROCHLORPERAZINE MALEATE) TABLET [BRYANT RANCH PREPACK] | 100 | Current NDC, 1 package rows | 20240224_7e3aa80a-3a5f-4937-b5aa-4ce2aa6ece1b.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72162-2262-1 | 72162226201 | 100 TABLET in 1 BOTTLE (72162-2262-1) | 100 tablet | 1998-03-01 | No | No | Historical |