olmesartan medoxomil
- Product NDC
- 50090-6606
- 11-digit product format
- 500906606
- Labeler code
- 50090
- Product ID
- 50090-6606_63e7c4d9-eb3e-47da-8807-234bd7df2977
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- olmesartan medoxomil
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA207662
- Marketing category
- ANDA
- Marketing start
- 2017-04-27
- Substance
- OLMESARTAN MEDOXOMIL
- Active strength
- 20 mg/1
- Pharmacologic classes
- Angiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 6M97XTV3HD | OLMESARTAN MEDOXOMIL | 144689-63-4 | OLMESARTAN MEDOXOMIL |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 50090-6606-0 | 50090660600 | 90 TABLET, FILM COATED in 1 BOTTLE (50090-6606-0) | 2023-08-22 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| olmesartan medoxomil | A-S Medication Solutions | 2023-08-28 | HUMAN PRESCRIPTION DRUG LABEL | 1 |