Telmisartan
- Product NDC
- 63629-7230
- 11-digit product format
- 636297230
- Labeler code
- 63629
- Product ID
- 63629-7230_f2943b94-e2fe-40b2-a796-bcd04419190d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Telmisartan
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA203867
- Marketing category
- ANDA
- Marketing start
- 2015-02-06
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-7230-1 | 63629723001 | 90 TABLET in 1 BOTTLE (63629-7230-1) | 90 tablet | 2017-03-27 | 0000-00-00 | No | No | Current |
| 63629-7230-2 | 63629723002 | 30 TABLET in 1 BOTTLE (63629-7230-2) | 30 tablet | 2017-03-27 | 0000-00-00 | No | No | Current |