telmisartan and hydrochlorthiazide
- Product NDC
- 13668-161
- 11-digit product format
- 136680161
- Labeler code
- 13668
- Product ID
- 13668-161_314fbd55-3e17-4e63-9974-3b16e6b58b3b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- telmisartan and hydrochlorthiazide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Torrent Pharmaceuticals Limited
- Application
- ANDA201192
- Marketing category
- ANDA
- Marketing start
- 2014-02-25
- Marketing end
- 0000-00-00
- Substance
- HYDROCHLOROTHIAZIDE; TELMISARTAN
- Active strength
- 25 mg/1; mg/1
- Pharmacologic classes
- Angiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC], Increased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS]
- 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 |
|---|
| 13668-161-01 | 13668016101 | 100 TABLET in 1 BOTTLE (13668-161-01) | 100 tablet | 2014-02-25 | 0000-00-00 | No | No | Current |
| 13668-161-30 | 13668016130 | 30 TABLET in 1 BOTTLE (13668-161-30) | 30 tablet | 2014-02-25 | 0000-00-00 | No | No | Current |
| 13668-161-72 | 13668016172 | 30 TABLET in 1 CARTON (13668-161-72) | 30 tablet | 2014-02-25 | 0000-00-00 | No | No | Current |
| 13668-161-74 | 13668016174 | 100 TABLET in 1 CARTON (13668-161-74) | 100 tablet | 2014-02-25 | 0000-00-00 | No | No | Current |