Famotidine
NDC 55111-118, Famotidine, tablet, from Dr.Reddys Laboratories Limited.
- Product NDC
- 55111-118
- Status
- Listed
- Labeler
- Dr.Reddys Laboratories Limited
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN OTC DRUG
- Marketing category
- ANDA
- Application
- ANDA077367
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/55111-118 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- FAMOTIDINE10 mg/1
Pharmacologic classes
Histamine H2 Receptor Antagonists [MoA]; Histamine-2 Receptor Antagonist [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 55111-118-04 | 55111011804 | 1 BOTTLE in 1 CARTON (55111-118-04) / 120 TABLET in 1 BOTTLE |
| 55111-118-12 | 55111011812 | 1 BLISTER PACK in 1 CARTON (55111-118-12) / 12 TABLET in 1 BLISTER PACK |
| 55111-118-18 | 55111011818 | 1 BOTTLE in 1 CARTON (55111-118-18) / 180 TABLET in 1 BOTTLE |
| 55111-118-24 | 55111011824 | 4 BLISTER PACK in 1 CARTON (55111-118-24) / 6 TABLET in 1 BLISTER PACK |
| 55111-118-30 | 55111011830 | 1 BOTTLE in 1 CARTON (55111-118-30) / 30 TABLET in 1 BOTTLE |
| 55111-118-35 | 55111011835 | 3 BLISTER PACK in 1 CARTON (55111-118-35) / 6 TABLET in 1 BLISTER PACK |
| 55111-118-40 | 55111011840 | 1 BOTTLE in 1 CARTON (55111-118-40) / 40 TABLET in 1 BOTTLE |
| 55111-118-60 | 55111011860 | 1 BOTTLE in 1 CARTON (55111-118-60) / 60 TABLET in 1 BOTTLE |
| 55111-118-79 | 55111011879 | 1 BLISTER PACK in 1 CARTON (55111-118-79) / 10 TABLET in 1 BLISTER PACK |
| 55111-118-81 | 55111011881 | 3 BLISTER PACK in 1 CARTON (55111-118-81) / 10 TABLET in 1 BLISTER PACK |
| 55111-118-90 | 55111011890 | 1 BOTTLE in 1 CARTON (55111-118-90) / 90 TABLET in 1 BOTTLE |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
NADAC price for package 55111011890
GET /v1/drugs/nadac/55111011890
Use it
Look up 55111-118 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/55111-118 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 55111-118. 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.