Famotidine
- Product NDC
- 0615-8301
- 11-digit product format
- 006158301
- Labeler code
- 0615
- Product ID
- 0615-8301_79066620-dee3-4323-b76b-547813369ce8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Famotidine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- NCS HealthCare of KY, LLC dba Vangard Labs
- Application
- ANDA075511
- Marketing category
- ANDA
- Marketing start
- 2001-04-16
- 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 |
|---|
| 0615-8301 | FAMOTIDINE TABLET, FILM COATED [NCS HEALTHCARE OF KY, LLC DBA VANGARD LABS] | 22 | Legacy NDC | 20241207_88f662fd-0d78-41f4-a26c-d831bea677d3.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0615-8301-39 | 00615830139 | 30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8301-39) | 2019-07-01 | 0000-00-00 | No | No | Current |