Fenofibrate 160 mg / 1 Tablet 30 Blister Pack
Reference details for licensed healthcare facility review and verification.
| NDC 11 | 60687-0864-21 |
|---|---|
| Product NDC | 60687-0864 |
| Generic Drug Name | Fenofibrate |
| Brand Name | Fenofibrate |
| Manufacturer | American Health Packaging |
| Strength | 160 mg / 1 |
| Dosage Form | Tablet |
| Drug Type | Oral |
| Package Quantity | 30 Blister Pack |
| Package Description | 30 BLISTER PACK in 1 CARTON (60687-864-21) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-864-11) |
| Active Ingredients | Fenofibrate |
| Marketing Category | ANDA |
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NDC snapshot
Fenofibrate 160 mg / 1 Tablet is tracked under NDC 60687-0864-21 and rolls up into product family 60687-0864. Use this page to review package-level identifiers before comparing related family pages or starting a quote review.
- Package configuration: 30 Blister Pack.
- Manufacturer: American Health Packaging.
- 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.
Potential alternatives with matching presentation
Open the comparison hub or review package-level listings from 2 product-NDC families with matching normalized presentation details. Review each product detail page before treating any item as a true alternative.
Fenofibrate 160 mg / 1 Tablet 30 Blister Pack, NDC 60687-0864-21, is a American Health Packaging 160 mg / 1 tablet presentation packaged as 30 Blister Pack.
NDC search formats
- Canonical NDC 11: 60687-0864-21
- Digits-only NDC 11: 60687086421
- Possible 10-digit display format: 60687-864-21 (6068786421)
Helpful product links
- Search by brand name: Fenofibrate
- NDC 11: 60687-0864-21
- Product family NDC: 60687-0864
- VA classification code: CV350
- VA classification code description: ANTILIPEMIC AGENTS
- CMOP ID: F0272
- VUID: 4015682