Famotidine
NDC 58602-706, Famotidine, tablet, film coated, from Aurohealth LLC.
- Product NDC
- 58602-706
- Status
- Listed
- Labeler
- Aurohealth LLC
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN OTC DRUG
- Marketing category
- ANDA
- Application
- ANDA206531
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/58602-706 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- FAMOTIDINE20 mg/1
Pharmacologic classes
Histamine H2 Receptor Antagonists [MoA]; Histamine-2 Receptor Antagonist [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 58602-706-14 | 58602070614 | 1 BOTTLE in 1 CARTON (58602-706-14) / 50 TABLET, FILM COATED in 1 BOTTLE |
| 58602-706-15 | 58602070615 | 2 BLISTER PACK in 1 CARTON (58602-706-15) / 8 TABLET, FILM COATED in 1 BLISTER PACK |
| 58602-706-16 | 58602070616 | 1 BOTTLE in 1 CARTON (58602-706-16) / 65 TABLET, FILM COATED in 1 BOTTLE |
| 58602-706-18 | 58602070618 | 1 BOTTLE in 1 CARTON (58602-706-18) / 80 TABLET, FILM COATED in 1 BOTTLE |
| 58602-706-19 | 58602070619 | 1 BOTTLE in 1 CARTON (58602-706-19) / 90 TABLET, FILM COATED in 1 BOTTLE |
| 58602-706-21 | 58602070621 | 1 BOTTLE in 1 CARTON (58602-706-21) / 100 TABLET, FILM COATED in 1 BOTTLE |
| 58602-706-34 | 58602070634 | 1 BOTTLE in 1 CARTON (58602-706-34) / 200 TABLET, FILM COATED in 1 BOTTLE |
| 58602-706-39 | 58602070639 | 1 BOTTLE in 1 CARTON (58602-706-39) / 365 TABLET, FILM COATED in 1 BOTTLE |
| 58602-706-40 | 58602070640 | 1 BOTTLE in 1 CARTON (58602-706-40) / 500 TABLET, FILM COATED in 1 BOTTLE |
| 58602-706-41 | 58602070641 | 1000 TABLET, FILM COATED in 1 BOTTLE (58602-706-41) |
| 58602-706-44 | 58602070644 | 1 BOTTLE in 1 CARTON (58602-706-44) / 400 TABLET, FILM COATED in 1 BOTTLE |
| 58602-706-47 | 58602070647 | 1 BOTTLE in 1 CARTON (58602-706-47) / 75 TABLET, FILM COATED in 1 BOTTLE |
| 58602-706-50 | 58602070650 | 1 BOTTLE in 1 CARTON (58602-706-50) / 85 TABLET, FILM COATED in 1 BOTTLE |
| 58602-706-53 | 58602070653 | 1 BOTTLE in 1 CARTON (58602-706-53) / 25 TABLET, FILM COATED in 1 BOTTLE |
| 58602-706-54 | 58602070654 | 1 BOTTLE in 1 CARTON (58602-706-54) / 70 TABLET, FILM COATED in 1 BOTTLE |
| 58602-706-56 | 58602070656 | 1 BOTTLE in 1 CARTON (58602-706-56) / 35 TABLET, FILM COATED in 1 BOTTLE |
| 58602-706-62 | 58602070662 | 5 BLISTER PACK in 1 CARTON (58602-706-62) / 5 TABLET, FILM COATED in 1 BLISTER PACK (58602-706-60) |
| 58602-706-79 | 58602070679 | 1 BLISTER PACK in 1 CARTON (58602-706-79) / 8 TABLET, FILM COATED in 1 BLISTER PACK |
| 58602-706-88 | 58602070688 | 750 TABLET, FILM COATED in 1 BOTTLE (58602-706-88) |
| 58602-706-94 | 58602070694 | 100 TABLET, FILM COATED in 1 BOTTLE (58602-706-94) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
No FDA label, Medicare Part B payment limit or NADAC price is linked to this product.
Use it
Look up 58602-706 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/58602-706 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 58602-706. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.