Pravastatin Sodium
- Product NDC
- 60687-169
- 11-digit product format
- 606870169
- Labeler code
- 60687
- Product ID
- 60687-169_eb03dc92-69fc-25fd-e053-2a95a90a4fa9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Pravastatin Sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- American Health Packaging
- Application
- ANDA077987
- Marketing category
- ANDA
- Marketing start
- 2016-07-25
- Marketing end
- 0000-00-00
- Substance
- PRAVASTATIN SODIUM
- Active strength
- 10 mg/1
- Pharmacologic classes
- HMG-CoA Reductase Inhibitor [EPC], Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 60687-169-01 | Pravastatin Sodium | 100 in 1 BOX, UNIT-DOSE | TABLET | 100 | | 14 |
| 60687-169-11 | Pravastatin Sodium | 1 in 1 BLISTER PACK | TABLET | 1 | | 14 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 60687-169 | PRAVASTATIN SODIUM TABLET [AMERICAN HEALTH PACKAGING] | 14 | Legacy NDC, 2 package rows | 20250207_056475c8-59c2-469c-9175-7162065726f5.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 |
|---|
| 60687-169-01 | 60687016901 | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-169-01) > 1 TABLET in 1 BLISTER PACK (60687-169-11) | 100 blister pack | 2016-07-25 | 0000-00-00 | No | No | Current |
| 60687-169-11 | 60687016911 | 1 in 1 BLISTER PACK | | | | | | Historical |