Altoprev
- Product NDC
- 70515-629
- 11-digit product format
- 705150629
- Labeler code
- 70515
- Product ID
- 70515-629_6ae2aacf-9571-4194-ac9a-14e29cd9061a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- lovastatin
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Covis Pharma US, Inc
- Application
- NDA021316
- Marketing category
- NDA
- Marketing start
- 2016-05-01
- Marketing end
- 0000-00-00
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70515-629 | ALTOPREV (LOVASTATIN) TABLET, EXTENDED RELEASE [COVIS PHARMA US, INC] | 8 | Legacy NDC | 20250115_8c0db100-5df9-49c3-8af9-1bc03ae609b9.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70515-629-30 | 70515062930 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70515-629-30) | 2016-05-01 | 0000-00-00 | No | No | Current |