Famotidine
- Product NDC
- 60760-327
- 11-digit product format
- 607600327
- Labeler code
- 60760
- Product ID
- 60760-327_f06e9bc0-c293-c5ce-e053-2995a90a2113
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Famotidine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- St. Mary's Medical Park Pharmacy
- Application
- ANDA075805
- Marketing category
- ANDA
- Marketing start
- 2020-12-18
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 60760-327 | FAMOTIDINE TABLET [ST. MARY'S MEDICAL PARK PHARMACY] | 3 | Legacy NDC | 20221223_b710445a-74f7-b9d2-e053-2a95a90a7b30.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60760-327-07 | 60760032707 | 7 TABLET in 1 BOTTLE, PLASTIC (60760-327-07) | 7 tablet | 2020-12-18 | 0000-00-00 | No | No | Current |
| 60760-327-60 | 60760032760 | 60 TABLET in 1 BOTTLE, PLASTIC (60760-327-60) | 60 tablet | 2021-01-07 | 0000-00-00 | No | No | Current |