Famotidine 20 mg / 1 Tablet 750 Tablet, Film Coated
Reference details for licensed healthcare facility review and verification.
| NDC 11 | 58602-0706-88 |
|---|---|
| Product NDC | 58602-0706 |
| Generic Drug Name | Famotidine |
| Brand Name | Famotidine |
| Manufacturer | Aurohealth LLC |
| Strength | 20 mg / 1 |
| Dosage Form | Tablet |
| Drug Type | Oral |
| Package Quantity | 750 Tablet, Film Coated |
| Package Description | 750 TABLET, FILM COATED in 1 BOTTLE (58602-706-88) |
| Active Ingredients | Famotidine |
| Marketing Category | ANDA |
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NDC snapshot
Famotidine 20 mg / 1 Tablet is tracked under NDC 58602-0706-88 and rolls up into product family 58602-0706. Use this page to review package-level identifiers before comparing related family pages or starting a quote review.
- Package configuration: 750 Tablet, Film Coated.
- Manufacturer: Aurohealth LLC.
- Dosage form: Tablet.
- Family size: 20 indexed presentations.
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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.
Alternate presentations in this family
These nearby package-level pages can help healthcare teams compare related packaging or presentation differences inside the same product-NDC family.
Famotidine 20 mg / 1 Tablet 750 Tablet, Film Coated, NDC 58602-0706-88, is a Aurohealth LLC 20 mg / 1 tablet presentation packaged as 750 Tablet, Film Coated.
NDC search formats
- Canonical NDC 11: 58602-0706-88
- Digits-only NDC 11: 58602070688
- Possible 10-digit display format: 58602-706-88 (5860270688)
Helpful product links
- Search by brand name: Famotidine
- NDC 11: 58602-0706-88
- Product family NDC: 58602-0706
- Other package sizes in this family: 1 Blister Pack, 1 Bottle
- Compare related presentations: Famotidine 20 mg / 1 Tablet 1 Blister Pack, Famotidine 20 mg / 1 Tablet 1 Bottle, Famotidine 20 mg / 1 Tablet 1 Bottle, Famotidine 20 mg / 1 Tablet 1 Bottle, Famotidine 20 mg / 1 Tablet 1 Bottle