Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide 5 mg / 1; 12.5 mg / 1; 20 mg / 1 Tablet 30 Tablet, Film Coated
Reference details for licensed healthcare facility review and verification.
| NDC 11 | 00093-5005-56 |
|---|---|
| Product NDC | 00093-5005 |
| Generic Drug Name | Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide |
| Brand Name | Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide |
| Manufacturer | Teva Pharmaceuticals USA, Inc. |
| Strength | 5 mg / 1; 12.5 mg / 1; 20 mg / 1 |
| Dosage Form | Tablet |
| Drug Type | Oral |
| Package Quantity | 30 Tablet, Film Coated |
| Package Description | 30 TABLET, FILM COATED in 1 BOTTLE (0093-5005-56) |
| Active Ingredients | Amlodipine Besylate; Hydrochlorothiazide; Olmesartan Medoxomil |
| Marketing Category | ANDA |
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NDC snapshot
Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide 5 mg / 1; 12.5 mg / 1; 20 mg / 1 Tablet is tracked under NDC 00093-5005-56 and rolls up into product family 00093-5005. 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: Teva Pharmaceuticals USA, Inc..
- Dosage form: Tablet.
- Family size: 1 indexed presentation.
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Official references
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Potential alternatives with matching presentation
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Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide 5 mg / 1; 12.5 mg / 1; 20 mg / 1 Tablet 30 Tablet, Film Coated, NDC 00093-5005-56, is a Teva Pharmaceuticals USA, Inc. 5 mg / 1; 12.5 mg / 1; 20 mg / 1 tablet presentation packaged as 30 Tablet, Film Coated.
NDC search formats
- Canonical NDC 11: 00093-5005-56
- Digits-only NDC 11: 00093500556
- Possible 10-digit display format: 0093-5005-56 (0093500556)
Helpful product links
- Search by brand name: Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide
- NDC 11: 00093-5005-56
- Product family NDC: 00093-5005
- VA classification code: CV400
- VA classification code description: ANTIHYPERTENSIVE COMBINATIONS
- CMOP ID: A1551
- VUID: 4030078