FDA NDC Directory · JSON-LD · Markdown
NDC 0069-7232 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED
| Generic name | amlodipine and atorvastatin |
|---|---|
| Labeler / Manufacturer | Pfizer Laboratories Div Pfizer Inc |
| Marketing category | New Drug Application (innovator) · App NDA021540 |
| Dosage form / route | TABLET, FILM COATED · ORAL |
| Active ingredients | AMLODIPINE BESYLATE (10 mg/1) ATORVASTATIN CALCIUM TRIHYDRATE (20 mg/1) |
| Marketing started | 20220831 |
| Package count | 1 |
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