TELMISARTAN
- Product NDC
- 13668-156
- 11-digit product format
- 136680156
- Labeler code
- 13668
- Product ID
- 13668-156_d91a8568-cce8-6a13-e053-2995a90ab1b6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- TELMISARTAN
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Torrent Pharmaceuticals Limited
- Application
- ANDA203171
- Marketing category
- ANDA
- Marketing start
- 2014-07-07
- Marketing end
- 0000-00-00
- 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
- 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 |
|---|
| 13668-156-01 | 13668015601 | 100 TABLET in 1 BOTTLE (13668-156-01) | 100 tablet | 2014-07-07 | 0000-00-00 | No | No | Current |
| 13668-156-30 | 13668015630 | 30 TABLET in 1 BOTTLE (13668-156-30) | 30 tablet | 2014-07-07 | 0000-00-00 | No | No | Current |
| 13668-156-72 | 13668015672 | 30 TABLET in 1 CARTON (13668-156-72) | 30 tablet | 2014-07-07 | 0000-00-00 | No | No | Current |
| 13668-156-74 | 13668015674 | 100 TABLET in 1 CARTON (13668-156-74) | 100 tablet | 2014-07-07 | 0000-00-00 | No | No | Current |