Famotidine
- Product NDC
- 70518-1877
- 11-digit product format
- 705181877
- Labeler code
- 70518
- Product ID
- 70518-1877_d34a3805-305c-0a5a-e053-2a95a90a366d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Famotidine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA075511
- Marketing category
- ANDA
- Marketing start
- 2019-02-15
- 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#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70518-1877 | FAMOTIDINE TABLET, FILM COATED [REMEDYREPACK INC.] | 10 | Legacy NDC | 20250302_cfbd1236-05bd-4dae-a094-d738f3139cb5.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-1877-1 | 70518187701 | 60 TABLET, FILM COATED in 1 BLISTER PACK (70518-1877-1) | 2021-12-15 | 0000-00-00 | No | No | Current |