Famotidine
- Product NDC
- 70518-0163
- 11-digit product format
- 705180163
- Labeler code
- 70518
- Product ID
- 70518-0163_e6d7bbe5-1678-162e-e053-2a95a90ad81d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Famotidine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA075511
- Marketing category
- ANDA
- Marketing start
- 2017-01-20
- 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
- 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 |
|---|
| 70518-0163 | FAMOTIDINE TABLET, FILM COATED [REMEDYREPACK INC.] | 19 | Legacy NDC | 20250529_3c32dd69-8211-4ec1-87d8-75e9dade14a1.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-0163-0 | 70518016300 | 30 TABLET, FILM COATED in 1 BOTTLE (70518-0163-0) | 2017-01-20 | 0000-00-00 | No | No | Current |
| 70518-0163-1 | 70518016301 | 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-0163-1) | 2017-02-02 | 0000-00-00 | No | No | Current |
| 70518-0163-2 | 70518016302 | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-0163-2) | 2018-08-01 | 0000-00-00 | No | No | Current |