Lovastatin
- Product NDC
- 50090-3216
- 11-digit product format
- 500903216
- Labeler code
- 50090
- Product ID
- 50090-3216_63db6524-2ace-4bd6-9758-537b4960c754
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lovastatin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA075551
- Marketing category
- ANDA
- Marketing start
- 2001-12-17
- Marketing end
- 0000-00-00
- Substance
- LOVASTATIN
- Active strength
- 40 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
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 |
|---|
| 50090-3216-0 | Lovastatin | 30 in 1 BOTTLE | TABLET | 30 | | 8 |
| 50090-3216-2 | Lovastatin | 90 in 1 BOTTLE, PLASTIC | TABLET | 90 | | 8 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-3216 | LOVASTATIN TABLET [A-S MEDICATION SOLUTIONS] | 8 | Legacy NDC, 2 package rows | 20241215_4ff981e8-5c86-4b86-baa1-825551905ed8.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 |
|---|
| 50090-3216-0 | 50090321600 | 30 TABLET in 1 BOTTLE (50090-3216-0) | 30 tablet | 2017-11-29 | 0000-00-00 | No | No | Current |
| 50090-3216-2 | 50090321602 | 90 TABLET in 1 BOTTLE, PLASTIC (50090-3216-2) | 90 tablet | 2014-11-28 | 0000-00-00 | No | No | Current |