Olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide 5 mg / 1; 25 mg / 1; 40 mg / 1 Tablet 30 Tablet, Film Coated
Reference details for licensed healthcare facility review and verification.
| NDC 11 | 70518-4165-00 |
|---|---|
| Product NDC | 70518-4165 |
| Generic Drug Name | olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide |
| Brand Name | olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide |
| Manufacturer | Remedyrepack Inc. |
| Strength | 5 mg / 1; 25 mg / 1; 40 mg / 1 |
| Dosage Form | Tablet |
| Drug Type | Oral |
| Package Quantity | 30 Tablet, Film Coated |
| Package Description | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4165-0) |
| Active Ingredients | Amlodipine Besylate; Hydrochlorothiazide; Olmesartan Medoxomil |
| Marketing Category | ANDA |
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NDC snapshot
olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide 5 mg / 1; 25 mg / 1; 40 mg / 1 Tablet is tracked under NDC 70518-4165-00 and rolls up into product family 70518-4165. Use this page to review package-level identifiers before comparing related family pages or starting a quote review.
- Package configuration: 30 Tablet, Film Coated.
- Manufacturer: Remedyrepack Inc..
- Dosage form: Tablet.
- Family size: 1 indexed presentation.
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Official references
Use official labeling and directory references to confirm presentation details while your team reviews the PRN catalog entry and related sourcing paths.
Olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide 5 mg / 1; 25 mg / 1; 40 mg / 1 Tablet 30 Tablet, Film Coated, NDC 70518-4165-00, is a Remedyrepack Inc. 5 mg / 1; 25 mg / 1; 40 mg / 1 tablet presentation packaged as 30 Tablet, Film Coated.
NDC search formats
- Canonical NDC 11: 70518-4165-00
- Digits-only NDC 11: 70518416500
- Possible 10-digit display format: 70518-4165-0 (7051841650)
Helpful product links
- Search by brand name: olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide
- NDC 11: 70518-4165-00
- Product family NDC: 70518-4165