Famotidine
- Product NDC
- 71205-535
- 11-digit product format
- 712050535
- Labeler code
- 71205
- Product ID
- 71205-535_37ca9d4f-3fed-421a-a18f-a9954c00a90c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Famotidine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA206530
- Marketing category
- ANDA
- Marketing start
- 2015-12-22
- Substance
- FAMOTIDINE
- Active strength
- 20 mg/1
- Pharmacologic classes
- Histamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 5QZO15J2Z8 | FAMOTIDINE | 76824-35-6 | FAMOTIDINE |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 71205-535-06 | 71205053506 | 6 TABLET, FILM COATED in 1 BOTTLE (71205-535-06) | 2021-02-24 | No | No | Historical |
| 71205-535-10 | 71205053510 | 10 TABLET, FILM COATED in 1 BOTTLE (71205-535-10) | 2021-02-24 | No | No | Historical |
| 71205-535-30 | 71205053530 | 30 TABLET, FILM COATED in 1 BOTTLE (71205-535-30) | 2021-02-16 | No | No | Historical |
| 71205-535-60 | 71205053560 | 60 TABLET, FILM COATED in 1 BOTTLE (71205-535-60) | 2021-02-16 | No | No | Historical |
| 71205-535-78 | 71205053578 | 180 TABLET, FILM COATED in 1 BOTTLE (71205-535-78) | 2024-09-06 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Famotidine | Proficient Rx LP | 2024-09-01 | HUMAN PRESCRIPTION DRUG LABEL | 4 |