Famotidine
- Product NDC
- 70518-3301
- 11-digit product format
- 705183301
- Labeler code
- 70518
- Product ID
- 70518-3301_d3be7b6a-8a81-98e7-e053-2995a90a08aa
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Famotidine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA206530
- Marketing category
- ANDA
- Marketing start
- 2021-12-21
- 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-3301-0 | 70518330100 | 28 TABLET, FILM COATED in 1 BLISTER PACK (70518-3301-0) | 2021-12-21 | 0000-00-00 | No | No | Current |