Pravastatin sodium
- Product NDC
- 63187-732
- 11-digit product format
- 631870732
- Labeler code
- 63187
- Product ID
- 63187-732_34dcede0-61f8-4aaa-b409-0e7d5c9e6f02
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Pravastatin sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA076939
- Marketing category
- ANDA
- Marketing start
- 2006-10-23
- Marketing end
- 0000-00-00
- Substance
- PRAVASTATIN SODIUM
- Active strength
- 40 mg/1
- Pharmacologic classes
- HMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63187-732 | PRAVASTATIN SODIUM TABLET [PROFICIENT RX LP] | 3 | Legacy NDC | 20191121_28b97a67-44d8-4db0-b166-60f096d409f5.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63187-732-30 | 63187073230 | 30 TABLET in 1 BOTTLE (63187-732-30) | 30 tablet | 2016-07-01 | 0000-00-00 | No | No | Current |
| 63187-732-60 | 63187073260 | 60 TABLET in 1 BOTTLE (63187-732-60) | 60 tablet | 2016-07-01 | 0000-00-00 | No | No | Current |
| 63187-732-90 | 63187073290 | 90 TABLET in 1 BOTTLE (63187-732-90) | 90 tablet | 2016-07-01 | 0000-00-00 | No | No | Current |