Telmisartan
- Product NDC
- 72162-2440
- 11-digit product format
- 721622440
- Labeler code
- 72162
- Product ID
- 72162-2440_7d7f8f3a-ecdf-4ec9-99ca-512b339baf4b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Telmisartan
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA208605
- Marketing category
- ANDA
- Marketing start
- 2015-02-05
- Substance
- TELMISARTAN
- Active strength
- 80 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 |
|---|
| 72162-2440-3 | 72162244003 | 30 TABLET in 1 BOTTLE (72162-2440-3) | 30 tablet | 2024-12-23 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Telmisartan | Bryant Ranch Prepack | 2024-12-23 | HUMAN PRESCRIPTION DRUG LABEL | 100 |