Telmisartan
- Product NDC
- 0781-5374
- 11-digit product format
- 007815374
- Labeler code
- 0781
- Product ID
- 0781-5374_616e4c7d-2752-4514-ba48-d8ba645f6baf
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Telmisartan
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Sandoz Inc
- Application
- ANDA203867
- Marketing category
- ANDA
- Marketing start
- 2015-02-06
- 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 |
|---|
| 0781-5374-06 | 00781537406 | 10 TABLET in 1 BLISTER PACK (0781-5374-06) | 10 tablet | 2015-02-06 | 0000-00-00 | No | No | Current |
| 0781-5374-64 | 00781537464 | 30 TABLET in 1 CARTON (0781-5374-64) | 30 tablet | 2015-02-06 | 0000-00-00 | No | No | Current |