Famotidine
- Product NDC
- 70934-540
- 11-digit product format
- 709340540
- Labeler code
- 70934
- Product ID
- 70934-540_ad2c100e-382c-49c2-e053-2995a90a5fc7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Famotidine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. dba Northwind Pharmaceuticals
- Application
- ANDA078916
- Marketing category
- ANDA
- Marketing start
- 2020-02-13
- Marketing end
- 0000-00-00
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70934-540-20 | 70934054020 | 20 TABLET in 1 BOTTLE, PLASTIC (70934-540-20) | 20 tablet | 2020-02-13 | 0000-00-00 | No | No | Current |
| 70934-540-30 | 70934054030 | 30 TABLET in 1 BOTTLE, PLASTIC (70934-540-30) | 30 tablet | 2020-02-13 | 0000-00-00 | No | No | Current |
| 70934-540-60 | 70934054060 | 60 TABLET in 1 BOTTLE, PLASTIC (70934-540-60) | 60 tablet | 2020-02-19 | 0000-00-00 | No | No | Current |