FDA NDC Directory · JSON-LD · Markdown
NDC 0093-0018 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED
| Labeler / Manufacturer | Teva Pharmaceuticals USA, Inc. |
|---|---|
| Marketing category | Abbreviated NDA (generic) · App ANDA077006 |
| Dosage form / route | TABLET, FILM COATED · ORAL |
| Active ingredients | TOLTERODINE TARTRATE (2 mg/1) |
| Marketing started | 20151101 |
| Package count | 2 |
Source: openFDA. Public-domain (CC0).