Micardis
- Product NDC
- 0597-0039
- 11-digit product format
- 005970039
- Labeler code
- 0597
- Product ID
- 0597-0039_40d4dcd9-5170-4685-bee8-4127d0bac0d0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- telmisartan
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Boehringer Ingelheim Pharmaceuticals, Inc.
- Application
- NDA020850
- Marketing category
- NDA
- Marketing start
- 2000-12-01
- 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
- 2024-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0597-0039-37 | Micardis | 10 in 1 BLISTER PACK | TABLET | 10 | | 31 |
| 0597-0039-37 | Micardis | 3 in 1 CARTON | TABLET | 3 | | 31 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0597-0039 | MICARDIS (TELMISARTAN) TABLET [BOEHRINGER INGELHEIM PHARMACEUTICALS, INC.] | 31 | Legacy NDC, 2 package rows | 20250523_cfb9309f-e0df-4a55-9542-0e869fce05fb.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0597-0039-37 | 00597003937 | 3 BLISTER PACK in 1 CARTON (0597-0039-37) > 10 TABLET in 1 BLISTER PACK | 3 blister pack | 2000-12-01 | 0000-00-00 | No | No | Current |