Famotidine
- Product NDC
- 49999-230
- 11-digit product format
- 499990230
- Labeler code
- 49999
- Product ID
- 49999-230_9dfd849a-bbc6-430b-a61b-d0ba3a265f03
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Famotidine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA075805
- Marketing category
- ANDA
- Marketing start
- 2009-12-31
- 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
- 2022-12-31
- 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 |
|---|
| 49999-230-30 | 49999023030 | 30 TABLET in 1 BOTTLE (49999-230-30) | 30 tablet | 2009-12-31 | 0000-00-00 | No | No | Current |