Lovastatin
- Product NDC
- 50090-0761
- 11-digit product format
- 500900761
- Labeler code
- 50090
- Product ID
- 50090-0761_a20c5e33-0bdf-466b-a0ad-cef977afdc41
- 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
- 40 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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Lovastatin
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| LOVASTATIN | 40 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 9LHU78OQFD |
| Rxcui | 197905 |
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 |
|---|
| 50090-0761-0 | Lovastatin | 30 in 1 BOTTLE | TABLET | 30 | | 16 |
| 50090-0761-2 | Lovastatin | 90 in 1 BOTTLE | TABLET | 90 | | 16 |
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 |
|---|
| 50090-0761-0 | 50090076100 | 30 TABLET in 1 BOTTLE (50090-0761-0) | 30 tablet | 2014-11-28 | 0000-00-00 | No | No | Current |
| 50090-0761-2 | 50090076102 | 90 TABLET in 1 BOTTLE (50090-0761-2) | 90 tablet | 2019-10-14 | 0000-00-00 | No | No | Current |