Atorvastatin calcium
- Product NDC
- 50090-5916
- 11-digit product format
- 500905916
- Labeler code
- 50090
- Product ID
- 50090-5916_4bc75cbf-38af-41a0-b269-dc9829a6466c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Atorvastatin calcium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA211933
- Marketing category
- ANDA
- Marketing start
- 2019-02-08
- Marketing end
- 0000-00-00
- Substance
- ATORVASTATIN CALCIUM TRIHYDRATE
- Active strength
- 40 mg/1
- Pharmacologic classes
- HMG-CoA Reductase Inhibitor [EPC], Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-5916-0 | 50090591600 | 90 TABLET, FILM COATED in 1 BOTTLE (50090-5916-0) | 2022-02-09 | 0000-00-00 | No | No | Current |