PROCHLORPERAZINE
- Product NDC
- 54348-114
- 11-digit product format
- 543480114
- Labeler code
- 54348
- Product ID
- 54348-114_ea92a656-4fd4-df01-e053-2a95a90a9de3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PROCHLORPERAZINE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- PharmPak, Inc.
- Application
- ANDA040268
- Marketing category
- ANDA
- Marketing start
- 2019-07-12
- Marketing end
- 0000-00-00
- Substance
- PROCHLORPERAZINE MALEATE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Phenothiazine [EPC], Phenothiazines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
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 |
|---|
| 54348-114-02 | PROCHLORPERAZINE | 2 in 1 BOTTLE | TABLET | 2 | | 2 |
| 54348-114-02 | PROCHLORPERAZINE | 1 in 1 BOX | TABLET | 1 | | 2 |
| 54348-114-04 | PROCHLORPERAZINE | 4 in 1 BOTTLE | TABLET | 4 | | 2 |
| 54348-114-04 | PROCHLORPERAZINE | 1 in 1 BOX | TABLET | 1 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 54348-114 | PROCHLORPERAZINE TABLET [PHARMPAK, INC.] | 2 | Legacy NDC, 4 package rows | 20221011_888f253f-1db1-45bc-8fc7-15f97ff0ba18.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 |
|---|
| 54348-114-02 | 54348011402 | 1 BOTTLE in 1 BOX (54348-114-02) > 2 TABLET in 1 BOTTLE | 1 bottle | 2019-07-12 | 0000-00-00 | No | No | Current |
| 54348-114-04 | 54348011404 | 1 BOTTLE in 1 BOX (54348-114-04) > 4 TABLET in 1 BOTTLE | 1 bottle | 2019-07-12 | 0000-00-00 | No | No | Current |