Famotidine
- Product NDC
- 60760-070
- 11-digit product format
- 607600070
- Labeler code
- 60760
- Product ID
- 60760-070_98d28bda-973b-ab1d-e053-2995a90a5ff7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Famotidine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- St. Mary's Medical Park Pharmacy
- Application
- ANDA078916
- Marketing category
- ANDA
- Marketing start
- 2019-02-27
- Marketing end
- 0000-00-00
- Substance
- FAMOTIDINE
- Active strength
- 40 mg/1
- Pharmacologic classes
- Histamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60760-070-07 | 60760007007 | 7 TABLET in 1 BOTTLE, PLASTIC (60760-070-07) | 7 tablet | 2019-12-03 | 0000-00-00 | No | No | Current |
| 60760-070-60 | 60760007060 | 60 TABLET in 1 BOTTLE, PLASTIC (60760-070-60) | 60 tablet | 2019-02-27 | 0000-00-00 | No | No | Current |