OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE 12.5 mg / 1; 40 mg / 1 Tablet 90 Tablet, Film Coated
Reference details for licensed healthcare facility review and verification.
| NDC 11 | 70518-4517-00 |
|---|---|
| Product NDC | 70518-4517 |
| Generic Drug Name | OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE |
| Brand Name | OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE |
| Manufacturer | Remedyrepack Inc. |
| Strength | 12.5 mg / 1; 40 mg / 1 |
| Dosage Form | Tablet |
| Drug Type | Oral |
| Package Quantity | 90 Tablet, Film Coated |
| Package Description | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4517-0) |
| Active Ingredients | Hydrochlorothiazide; Olmesartan Medoxomil |
| Marketing Category | ANDA |
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NDC snapshot
OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE 12.5 mg / 1; 40 mg / 1 Tablet is tracked under NDC 70518-4517-00 and rolls up into product family 70518-4517. Use this page to review package-level identifiers before comparing related family pages or starting a quote review.
- Package configuration: 90 Tablet, Film Coated.
- Manufacturer: Remedyrepack Inc..
- Dosage form: Tablet.
- Family size: 1 indexed presentation.
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Official references
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Potential alternatives with matching presentation
Open the comparison hub or review package-level listings from 14 product-NDC families with matching normalized presentation details. Review each product detail page before treating any item as a true alternative.
OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE 12.5 mg / 1; 40 mg / 1 Tablet 90 Tablet, Film Coated, NDC 70518-4517-00, is a Remedyrepack Inc. 12.5 mg / 1; 40 mg / 1 tablet presentation packaged as 90 Tablet, Film Coated.
NDC search formats
- Canonical NDC 11: 70518-4517-00
- Digits-only NDC 11: 70518451700
- Possible 10-digit display format: 70518-4517-0 (7051845170)
Helpful product links
- Search by brand name: OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE
- NDC 11: 70518-4517-00
- Product family NDC: 70518-4517