Telmisartan
- Product NDC
- 31722-804
- 11-digit product format
- 317220804
- Labeler code
- 31722
- Product ID
- 31722-804_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
- 80 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 |
|---|
| 31722-804-31 | 31722080431 | 10 TABLET in 1 BLISTER PACK (31722-804-31) | 10 tablet | 2016-04-25 | 0000-00-00 | No | No | Current |
| 31722-804-32 | 31722080432 | 15 TABLET in 1 CARTON (31722-804-32) | 15 tablet | 2016-04-25 | 0000-00-00 | No | No | Current |
| 31722-804-33 | 31722080433 | 10 TABLET in 1 BLISTER PACK (31722-804-33) | 10 tablet | 2016-04-25 | 0000-00-00 | No | No | Current |
| 31722-804-34 | 31722080434 | 15 TABLET in 1 CARTON (31722-804-34) | 15 tablet | 2016-04-25 | 0000-00-00 | No | No | Current |
| 31722-804-35 | 31722080435 | 3 TABLET in 1 CARTON (31722-804-35) | 3 tablet | 2016-04-25 | 0000-00-00 | No | No | Current |
| 31722-804-36 | 31722080436 | 10 TABLET in 1 BLISTER PACK (31722-804-36) | 10 tablet | 2016-04-25 | 0000-00-00 | No | No | Current |
| 31722-804-37 | 31722080437 | 3 TABLET in 1 CARTON (31722-804-37) | 3 tablet | 2016-04-25 | 0000-00-00 | No | No | Current |