Telmisartan
- Product NDC
- 72606-507
- 11-digit product format
- 726060507
- Labeler code
- 72606
- Product ID
- 72606-507_4eca88a5-21d9-4a8c-b4e3-632ff8873bd6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Telmisartan
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- CELLTRION USA, INC.
- Application
- ANDA078710
- Marketing category
- ANDA
- Marketing start
- 2020-11-23
- Marketing end
- 0000-00-00
- Substance
- TELMISARTAN
- Active strength
- 40 mg/1
- Pharmacologic classes
- Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 72606-507-02 | 72606050702 | 3 BLISTER PACK in 1 CARTON (72606-507-02) > 10 TABLET in 1 BLISTER PACK | 3 blister pack | 2020-11-23 | 0000-00-00 | No | No | Current |
| 72606-507-03 | 72606050703 | 30 TABLET in 1 BOTTLE (72606-507-03) | 30 tablet | 2020-11-23 | 0000-00-00 | No | No | Current |