Lovastatin
- Product NDC
- 83209-468
- 11-digit product format
- 832090468
- Labeler code
- 83209
- Product ID
- 83209-468_2eeb366e-7823-d98e-e063-6394a90a3b70
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- lovastatin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Boswell Pharmacy Services LLC d/b/a BPS Wholesale
- Application
- ANDA078296
- Marketing category
- ANDA
- Marketing start
- 2025-02-24
- Substance
- LOVASTATIN
- Active strength
- 20 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 | 20 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 9LHU78OQFD |
| Rxcui | 197904 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 83209-468-30 | Lovastatin | 30 in 1 BLISTER PACK | TABLET | 30 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 83209-468-30 | 83209046830 | 30 TABLET in 1 BLISTER PACK (83209-468-30) | 30 tablet | 2025-02-24 | No | No | Current |