telmisartan
- Product NDC
- 70518-3300
- 11-digit product format
- 705183300
- Labeler code
- 70518
- Product ID
- 70518-3300_e83e39e4-0159-7852-e053-2995a90a63d0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- telmisartan
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA203325
- Marketing category
- ANDA
- Marketing start
- 2021-12-20
- 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
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 | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-3300-0 | 70518330000 | 30 BLISTER PACK in 1 CARTON (70518-3300-0) > 1 TABLET in 1 BLISTER PACK | 30 blister pack | 2021-12-20 | 0000-00-00 | No | No | Current |