Famotidine
- Product NDC
- 70934-819
- 11-digit product format
- 709340819
- Labeler code
- 70934
- Product ID
- 70934-819_bb79a9f5-e6bd-b7af-e053-2995a90a314b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Famotidine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. DBA Northwind Pharmaceuticals
- Application
- ANDA075511
- Marketing category
- ANDA
- Marketing start
- 2021-01-26
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70934-819-30 | 70934081930 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-819-30) | 2021-01-26 | 0000-00-00 | No | No | Current |
| 70934-819-60 | 70934081960 | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-819-60) | 2021-02-16 | 0000-00-00 | No | No | Current |