Amlodipine and Olmesartan Medoxomil
- Product NDC
- 50090-7863
- 11-digit product format
- 500907863
- Labeler code
- 50090
- Product ID
- 50090-7863_d7534eb1-2b9b-45ea-a35d-f1653a807a91
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amlodipine and Olmesartan Medoxomil
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA206906
- Marketing category
- ANDA
- Marketing start
- 2017-05-15
- Substance
- AMLODIPINE BESYLATE; OLMESARTAN MEDOXOMIL
- Active strength
- 5; 20 mg/1; mg/1
- Pharmacologic classes
- Angiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC], Calcium Channel Antagonists [MoA], Calcium Channel Blocker [EPC], Cytochrome P450 3A Inhibitors [MoA], Dihydropyridine Calcium Channel Blocker [EPC], Dihydropyridines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Amlodipine and Olmesartan Medoxomil
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| AMLODIPINE BESYLATE | 5 mg/1 |
| OLMESARTAN MEDOXOMIL | 20 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 864V2Q084H, 6M97XTV3HD |
| Rxcui | 730869 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50090-7863-0 | Amlodipine and Olmesartan Medoxomil | 30 in 1 BOTTLE | TABLET, FILM COATED | 30 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 50090-7863-0 | 50090786300 | 30 TABLET, FILM COATED in 1 BOTTLE (50090-7863-0) | 2026-01-22 | No | No | Historical |