Alendronate sodium 35 mg / 1 Tablet 3 Blister Pack
Reference details for licensed healthcare facility review and verification.
| NDC 11 | 69097-0223-76 |
|---|---|
| Product NDC | 69097-0223 |
| Generic Drug Name | Alendronate sodium |
| Brand Name | Alendronate Sodium |
| Manufacturer | Cipla USA Inc. |
| Strength | 35 mg / 1 |
| Dosage Form | Tablet |
| Drug Type | Oral |
| Package Quantity | 3 Blister Pack |
| Package Description | 3 BLISTER PACK in 1 CARTON (69097-223-76) / 4 TABLET in 1 BLISTER PACK (69097-223-16) |
| Active Ingredients | Alendronate Sodium |
| Marketing Category | ANDA |
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NDC snapshot
Alendronate sodium 35 mg / 1 Tablet is tracked under NDC 69097-0223-76 and rolls up into product family 69097-0223. Use this page to review package-level identifiers before comparing related family pages or starting a quote review.
- Package configuration: 3 Blister Pack.
- Manufacturer: Cipla USA 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.
Potential alternatives with matching presentation
Open the comparison hub or review package-level listings from 6 product-NDC families with matching normalized presentation details. Review each product detail page before treating any item as a true alternative.
Alendronate sodium 35 mg / 1 Tablet 3 Blister Pack, NDC 69097-0223-76, is a Cipla USA Inc. 35 mg / 1 tablet presentation packaged as 3 Blister Pack.
NDC search formats
- Canonical NDC 11: 69097-0223-76
- Digits-only NDC 11: 69097022376
- Possible 10-digit display format: 69097-223-76 (6909722376)
Helpful product links
- Search by brand name: Alendronate Sodium
- NDC 11: 69097-0223-76
- Product family NDC: 69097-0223
- VA classification code: HS900
- VA classification code description: HORMONES/SYNTHETICS/MODIFIERS,OTHER
- CMOP ID: A1069
- VUID: 4015143