Telmisartan
- Product NDC
- 31722-802
- 11-digit product format
- 317220802
- Labeler code
- 31722
- Product ID
- 31722-802_95dc7a73-2c00-4e39-813a-a3f94f5e1b4b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Telmisartan
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Camber Pharmaceuticals, Inc.
- Application
- ANDA205901
- Marketing category
- ANDA
- Marketing start
- 2016-04-25
- 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
- 2020-12-31
- 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 |
|---|
| 31722-802-31 | 31722080231 | 10 TABLET in 1 BLISTER PACK (31722-802-31) | 10 tablet | 2016-04-25 | 0000-00-00 | No | No | Current |
| 31722-802-32 | 31722080232 | 25 TABLET in 1 CARTON (31722-802-32) | 25 tablet | 2016-04-25 | 0000-00-00 | No | No | Current |
| 31722-802-33 | 31722080233 | 10 TABLET in 1 BLISTER PACK (31722-802-33) | 10 tablet | 2016-04-25 | 0000-00-00 | No | No | Current |
| 31722-802-34 | 31722080234 | 25 TABLET in 1 CARTON (31722-802-34) | 25 tablet | 2016-04-25 | 0000-00-00 | No | No | Current |
| 31722-802-35 | 31722080235 | 3 TABLET in 1 CARTON (31722-802-35) | 3 tablet | 2016-04-25 | 0000-00-00 | No | No | Current |
| 31722-802-36 | 31722080236 | 3 TABLET in 1 CARTON (31722-802-36) | 3 tablet | 2016-04-25 | 0000-00-00 | No | No | Current |