telmisartan
- Product NDC
- 72789-371
- 11-digit product format
- 727890371
- Labeler code
- 72789
- Product ID
- 72789-371_34184fdf-e74f-fa7f-e063-6294a90a66c3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- telmisartan
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA205150
- Marketing category
- ANDA
- Marketing start
- 2016-06-12
- Substance
- TELMISARTAN
- Active strength
- 20 mg/1
- Pharmacologic classes
- Angiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| U5SYW473RQ | TELMISARTAN | 144701-48-4 | TELMISARTAN |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72789-371-90 | 72789037190 | 90 TABLET in 1 BOTTLE, PLASTIC (72789-371-90) | 90 tablet | 2024-01-23 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| telmisartan | PD-Rx Pharmaceuticals, Inc. | 2025-05-01 | HUMAN PRESCRIPTION DRUG LABEL | 11 |