Atorvastatin Calcium
- Product NDC
- 51655-921
- 11-digit product format
- 516550921
- Labeler code
- 51655
- Product ID
- 51655-921_c924fcb5-f571-20fd-e053-2995a90a1115
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Atorvastatin Calcium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Northwind Pharmaceuticals
- Application
- ANDA091624
- Marketing category
- ANDA
- Marketing start
- 2020-07-07
- Marketing end
- 0000-00-00
- Substance
- ATORVASTATIN CALCIUM TRIHYDRATE
- Active strength
- 20 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 51655-921-52 | 51655092152 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-921-52) | 2020-07-07 | 0000-00-00 | No | No | Current |