Atorvastatin Calcium
- Product NDC
- 60760-829
- 11-digit product format
- 607600829
- Labeler code
- 60760
- Product ID
- 60760-829_ef53a855-a5df-8e3e-e053-2a95a90a19f6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Atorvastatin Calcium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- ST. MARY'S MEDICAL PARK PHARMACY
- Application
- ANDA076477
- Marketing category
- ANDA
- Marketing start
- 2022-11-08
- 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
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 60760-829 | ATORVASTATIN CALCIUM TABLET, FILM COATED [ST. MARY'S MEDICAL PARK PHARMACY] | 1 | Legacy NDC | 20221209_ef53a017-5a66-2334-e053-2995a90ae593.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60760-829-30 | 60760082930 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-829-30) | 2022-11-08 | 0000-00-00 | No | No | Current |