Lovastatin
- Product NDC
- 50090-3268
- 11-digit product format
- 500903268
- Labeler code
- 50090
- Product ID
- 50090-3268_b0495791-5afa-4a05-8e6f-5f58fefbee46
- 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
- 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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Lovastatin
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| LOVASTATIN | 10 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 9LHU78OQFD |
| Rxcui | 197903, 197905 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50090-3268-0 | Lovastatin | 30 in 1 BOTTLE | TABLET | 30 | | 8 |
| 50090-3268-1 | Lovastatin | 90 in 1 BOTTLE | TABLET | 90 | | 8 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-3268 | LOVASTATIN TABLET [A-S MEDICATION SOLUTIONS] | 8 | Current NDC, 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 | Sample | Exclude flag | Status |
|---|
| 50090-3268-0 | 50090326800 | 30 TABLET in 1 BOTTLE (50090-3268-0) | 30 tablet | 2018-04-06 | No | No | Historical |
| 50090-3268-1 | 50090326801 | 90 TABLET in 1 BOTTLE (50090-3268-1) | 90 tablet | 2017-11-17 | No | No | Historical |