Famotidine 20 mg / 1 Tablet 10 Blister Pack
Reference details for licensed healthcare facility review and verification.
| NDC 11 | 63739-0645-10 |
|---|---|
| Product NDC | 63739-0645 |
| Generic Drug Name | Famotidine |
| Brand Name | Famotidine |
| Manufacturer | Mckesson Corporation DBA SKY Packaginng |
| Strength | 20 mg / 1 |
| Dosage Form | Tablet |
| Drug Type | Oral |
| Package Quantity | 10 Blister Pack |
| Package Description | 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-645-10) / 10 TABLET in 1 BLISTER PACK |
| Active Ingredients | Famotidine |
| Marketing Category | ANDA |
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NDC snapshot
Famotidine 20 mg / 1 Tablet is tracked under NDC 63739-0645-10 and rolls up into product family 63739-0645. Use this page to review package-level identifiers before comparing related family pages or starting a quote review.
- Package configuration: 10 Blister Pack.
- Manufacturer: Mckesson Corporation DBA SKY Packaginng.
- 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.
Drug Shortage Information
Public sources show a strong exact DailyMed label for the NDC and a relevant FDA market-context page tied to famotidine’s role during the ranitidine withdrawal era.
Famotidine 20 mg / 1 Tablet 10 Blister Pack, NDC 63739-0645-10, is a Mckesson Corporation DBA SKY Packaginng 20 mg / 1 tablet presentation packaged as 10 Blister Pack. Historical public shortage information is available for this product reference.
NDC search formats
- Canonical NDC 11: 63739-0645-10
- Digits-only NDC 11: 63739064510
- Possible 10-digit display format: 63739-645-10 (6373964510)
Helpful product links
- Search by brand name: Famotidine
- NDC 11: 63739-0645-10
- Product family NDC: 63739-0645
- VA classification code: GA301
- VA classification code description: HISTAMINE ANTAGONISTS
- CMOP ID: F0219
- VUID: 4013936