atorvastatin calcium
- Product NDC
- 70377-029
- 11-digit product format
- 703770029
- Labeler code
- 70377
- Product ID
- 70377-029_c8ace345-ce52-482e-93b9-6b81fe40c1fd
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- atorvastatin calcium, film coated
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Biocon Pharma Inc.,
- Application
- ANDA209912
- Marketing category
- ANDA
- Marketing start
- 2018-06-18
- 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 Product Concepts#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70377-029 | ATORVASTATIN CALCIUM (ATORVASTATIN CALCIUM, FILM COATED) TABLET [BIOCON PHARMA INC.,] | 9 | Legacy NDC | 20220706_1daa6f20-a032-4541-939d-931f36a020dd.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70377-029-11 | 70377002911 | 90 TABLET in 1 BOTTLE (70377-029-11) | 90 tablet | 2018-06-18 | 0000-00-00 | No | No | Current |
| 70377-029-12 | 70377002912 | 500 TABLET in 1 BOTTLE (70377-029-12) | 500 tablet | 2018-06-18 | 0000-00-00 | No | No | Current |
| 70377-029-13 | 70377002913 | 1000 TABLET in 1 BOTTLE (70377-029-13) | 1000 tablet | 2018-06-18 | 0000-00-00 | No | No | Current |