Lovastatin
- Product NDC
- 70518-2425
- 11-digit product format
- 705182425
- Labeler code
- 70518
- Product ID
- 70518-2425_4a186a1c-0363-f64a-e063-6394a90a51eb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lovastatin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA075991
- Marketing category
- ANDA
- Marketing start
- 2019-11-18
- 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
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Lovastatin
- Listing expiration
- 2027-12-31
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#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70518-2425-0 | Lovastatin | 30 in 1 BLISTER PACK | TABLET | 30 | | 4 |
| 70518-2425-1 | Lovastatin | 90 in 1 BOTTLE, PLASTIC | TABLET | 90 | | 4 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 70518-2425-0 | 70518242500 | 30 in 1 BLISTER PACK | | | | | Historical |
| 70518-2425-1 | 70518242501 | 90 TABLET in 1 BOTTLE, PLASTIC (70518-2425-1) | 90 tablet | 2025-08-26 | No | No | Current |