Lovastatin
- Product NDC
- 50090-0757
- 11-digit product format
- 500900757
- Labeler code
- 50090
- Product ID
- 50090-0757_80023785-4b99-48c1-b757-c391056fe6fc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lovastatin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA075991
- Marketing category
- ANDA
- Marketing start
- 2002-11-25
- Substance
- LOVASTATIN
- Active strength
- 10 mg/1
- Pharmacologic classes
- HMG-CoA Reductase Inhibitor [EPC], Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
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 |
|---|
| 50090-0757-0 | Lovastatin | 30 in 1 BOTTLE | TABLET | 30 | | 20 |
| 50090-0757-1 | Lovastatin | 90 in 1 BOTTLE | TABLET | 90 | | 20 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-0757 | LOVASTATIN TABLET [A-S MEDICATION SOLUTIONS] | 20 | Current NDC, Legacy NDC, 2 package rows | 20230208_5e4555fe-c73c-44ff-973a-a5fd24122830.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-0757-0 | 50090075700 | 30 TABLET in 1 BOTTLE (50090-0757-0) | 30 tablet | 2014-11-28 | 0000-00-00 | No | No | Current |
| 50090-0757-1 | 50090075701 | 90 TABLET in 1 BOTTLE (50090-0757-1) | 90 tablet | 2014-11-28 | 0000-00-00 | No | No | Current |