Telmisartan
- Product NDC
- 50090-5489
- 11-digit product format
- 500905489
- Labeler code
- 50090
- Product ID
- 50090-5489_1bb809ec-819e-437b-ac3e-db251ed587fd
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- telmisartan
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA202397
- Marketing category
- ANDA
- Marketing start
- 2014-07-07
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50090-5489-0 | Telmisartan | 90 in 1 BOTTLE, PLASTIC | TABLET | 90 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-5489 | TELMISARTAN TABLET [A-S MEDICATION SOLUTIONS] | 2 | Legacy NDC, 1 package rows | 20210911_59bb2556-7add-49b5-8c04-eef5ff60c46a.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 |
|---|
| 50090-5489-0 | 50090548900 | 90 TABLET in 1 BOTTLE, PLASTIC (50090-5489-0) | 90 tablet | 2021-03-15 | 0000-00-00 | No | No | Current |