Amlodipine and Atorvastatin
- Product NDC
- 72162-2094
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amlodipine and Atorvastatin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA205199
- Marketing category
- ANDA
- Substance
- AMLODIPINE BESYLATE; ATORVASTATIN CALCIUM TRIHYDRATE
- Current FDA listing
- Yes
Related Records
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|---|---|---|---|---|
| 72162-2094-3 | 30 TABLET, FILM COATED in 1 BOTTLE (72162-2094-3) | 2026-03-20 | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|---|---|---|---|
| Amlodipine and Atorvastatin | Bryant Ranch Prepack | 2026-03-20 | HUMAN PRESCRIPTION DRUG LABEL | 104 |