TELMISARTAN
- Product NDC
- 71335-1841
- 11-digit product format
- 713351841
- Labeler code
- 71335
- Product ID
- 71335-1841_81c2ee77-f3ce-4366-a609-457442509457
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Telmisartan
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA207016
- Marketing category
- ANDA
- Marketing start
- 2018-01-01
- Marketing end
- 0000-00-00
- Substance
- TELMISARTAN
- Active strength
- 40 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 |
|---|
| 71335-1841-1 | 71335184101 | 30 TABLET in 1 BOTTLE (71335-1841-1) | 30 tablet | 2021-08-06 | 0000-00-00 | No | No | Current |
| 71335-1841-2 | 71335184102 | 90 TABLET in 1 BOTTLE (71335-1841-2) | 90 tablet | 2022-02-14 | 0000-00-00 | No | No | Current |