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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- telmisartan
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| TELMISARTAN | 20 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | U5SYW473RQ |
| Rxcui | 282755 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72789-371-90 | telmisartan | 90 in 1 BOTTLE, PLASTIC | TABLET | 90 | | 11 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72789-371 | TELMISARTAN TABLET [PD-RX PHARMACEUTICALS, INC.] | 11 | Current NDC, 1 package rows | 20250503_56a72ddf-c2a2-45ce-91b1-1fcfbff52c10.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| 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 | Current |