Famotidine
- Product NDC
- 55681-341
- 11-digit product format
- 556810341
- Labeler code
- 55681
- Product ID
- 55681-341_f7f1bb4e-df0e-8a7b-e053-6294a90a9c47
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Famotidine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- TWIN MED LLC
- Application
- ANDA215822
- Marketing category
- ANDA
- Marketing start
- 2022-01-28
- Substance
- FAMOTIDINE
- Active strength
- 10 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
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 55681-341-03 | Famotidine | 300 in 1 BOTTLE | TABLET, FILM COATED | 300 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 55681-341 | FAMOTIDINE TABLET, FILM COATED [TWIN MED LLC] | 1 | Current NDC, 1 package rows | 20230329_f7f1bb4e-df0d-8a7b-e053-6294a90a9c47.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 55681-341-03 | 55681034103 | 300 TABLET, FILM COATED in 1 BOTTLE (55681-341-03) | 2022-09-07 | No | No | Historical |