PRAVASTATIN SODIUM
- Product NDC
- 50090-3898
- 11-digit product format
- 500903898
- Labeler code
- 50090
- Product ID
- 50090-3898_de1b8af1-6c7f-44e5-8749-f270c89a5a79
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PRAVASTATIN SODIUM
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA207068
- Marketing category
- ANDA
- Marketing start
- 2017-02-16
- Marketing end
- 0000-00-00
- Substance
- PRAVASTATIN SODIUM
- Active strength
- 20 mg/1
- Pharmacologic classes
- HMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-3898 | PRAVASTATIN SODIUM TABLET [A-S MEDICATION SOLUTIONS] | 8 | Legacy NDC | 20240126_6c9bb49b-a8f1-432f-a1d0-27904b01c184.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-3898-0 | 50090389800 | 30 TABLET in 1 BOTTLE (50090-3898-0) | 30 tablet | 2018-12-04 | 0000-00-00 | No | No | Current |
| 50090-3898-1 | 50090389801 | 90 TABLET in 1 BOTTLE, PLASTIC (50090-3898-1) | 90 tablet | 2017-02-16 | 0000-00-00 | No | No | Current |