Famotidine
- Product NDC
- 69238-2090
- 11-digit product format
- 692382090
- Labeler code
- 69238
- Product ID
- 69238-2090_ddc06a12-1bc6-4006-ba9c-ed389599b532
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Famotidine
- Dosage form
- POWDER, FOR SUSPENSION
- Route
- ORAL
- Labeler
- Amneal Pharmaceuticals NY LLC
- Application
- ANDA216427
- Marketing category
- ANDA
- Marketing start
- 2022-08-05
- Substance
- FAMOTIDINE
- Active strength
- 40 mg/5mL
- 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 |
|---|
| 69238-2090-4 | Famotidine | 50 mL in 1 BOTTLE | POWDER, FOR SUSPENSION | 50 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 69238-2090 | FAMOTIDINE POWDER, FOR SUSPENSION [AMNEAL PHARMACEUTICALS NY LLC] | 6 | Current NDC, Legacy NDC, 1 package rows | 20231231_bb602b05-0ce6-4029-bd6e-291076e64efb.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 69238-2090-4 | 69238209004 | 50 mL in 1 BOTTLE (69238-2090-4) | 50 ml | 2022-08-05 | 0000-00-00 | No | No | Current |