Famotidine 20 mg / 1 Tablet 300 Tablet, Film Coated
Reference details for licensed healthcare facility review and verification.
| NDC 11 | 55681-0342-03 |
|---|---|
| Product NDC | 55681-0342 |
| Generic Drug Name | Famotidine |
| Brand Name | Famotidine |
| Manufacturer | Twin Med Llc |
| Strength | 20 mg / 1 |
| Dosage Form | Tablet |
| Drug Type | Oral |
| Package Quantity | 300 Tablet, Film Coated |
| Package Description | 300 TABLET, FILM COATED in 1 BOTTLE (55681-342-03) |
| Active Ingredients | Famotidine |
| Marketing Category | ANDA |
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NDC snapshot
Famotidine 20 mg / 1 Tablet is tracked under NDC 55681-0342-03 and rolls up into product family 55681-0342. Use this page to confirm the exact presentation before comparing related family pages or starting a quote review.
- Package configuration: 300 Tablet, Film Coated.
- Manufacturer: Twin Med Llc.
- 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.
Famotidine 20 mg / 1 Tablet 300 Tablet, Film Coated, NDC 55681-0342-03, is a Twin Med Llc 20 mg / 1 tablet presentation packaged as 300 Tablet, Film Coated.
NDC search formats
- Canonical NDC 11: 55681-0342-03
- Digits-only NDC 11: 55681034203
- Possible 10-digit display formats: 55681-342-03 (5568134203), 55681-0342-3 (5568103423)
Multiple 10-digit display-format aliases can map to the same stored 11-digit billing NDC, so these are shown as search aliases rather than a single asserted package format.
Helpful product links
- Search by brand name: Famotidine
- Exact NDC 11: 55681-0342-03
- Product family NDC: 55681-0342