telmisartan
- Product NDC
- 71335-0875
- 11-digit product format
- 713350875
- Labeler code
- 71335
- Product ID
- 71335-0875_7b7fc5fa-9322-4291-9d75-35a1e81b6b31
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- telmisartan
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA203325
- Marketing category
- ANDA
- Marketing start
- 2014-08-27
- Marketing end
- 0000-00-00
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71335-0875-1 | 71335087501 | 90 TABLET in 1 BOTTLE (71335-0875-1) | 90 tablet | 2018-06-21 | 0000-00-00 | No | No | Current |
| 71335-0875-2 | 71335087502 | 30 TABLET in 1 BOTTLE (71335-0875-2) | 30 tablet | 2019-01-08 | 0000-00-00 | No | No | Current |