Application 073582
- Type
- ANDA
- Sponsor
- SUN PHARM INDUSTRIES
Application Products#
Product, Drug, Ingredient table| Product | Drug | Ingredient | Form | Strength | Reference drug | Reference standard |
|---|
| 001 | ATENOLOL AND CHLORTHALIDONE | ATENOLOL; CHLORTHALIDONE | TABLET;ORAL | 100MG;25MG | No | No |
| 002 | ATENOLOL AND CHLORTHALIDONE | ATENOLOL; CHLORTHALIDONE | TABLET;ORAL | 50MG;25MG | No | No |
NDC Listings For This Application#
NDC, Name, Nonproprietary name table| NDC | Name | Nonproprietary name | Labeler | Marketing category | Status |
|---|
| 53489-531 | Atenolol and Chlorthalidone | Atenolol and Chlorthalidone | Mutual Pharmaceutical Company, Inc. | ANDA | Current |
| 53489-532 | Atenolol and Chlorthalidone | Atenolol and Chlorthalidone | Mutual Pharmaceutical Company, Inc. | ANDA | Current |