Famotidine
- Product NDC
- 71872-7220
- 11-digit product format
- 718727220
- Labeler code
- 71872
- Product ID
- 71872-7220_fadf58e6-92cd-d87b-e053-6394a90a966f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Famotidine
- Dosage form
- INJECTION
- Route
- INTRAVENOUS
- Labeler
- Medical Purchasing Solutions, LLC
- Application
- ANDA078642
- Marketing category
- ANDA
- Marketing start
- 2008-06-26
- Substance
- FAMOTIDINE
- Active strength
- 10 mg/mL
- 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 | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71872-7220-1 | 71872722001 | 1 VIAL in 1 BAG (71872-7220-1) / 2 mL in 1 VIAL | 1 vial | 2020-11-12 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| FAMOTIDINE INJECTION, USP | Medical Purchasing Solutions, LLC | 2023-05-04 | HUMAN PRESCRIPTION DRUG LABEL | 2 |