up and up famotidine
- Product NDC
- 11673-031
- 11-digit product format
- 116730031
- Labeler code
- 11673
- Product ID
- 11673-031_763d7c0c-950b-42ea-96e1-745e8445bb65
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Famotidine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Target Corporation
- Application
- ANDA075400
- Marketing category
- ANDA
- Marketing start
- 2015-03-13
- Marketing end
- 0000-00-00
- Substance
- FAMOTIDINE
- Active strength
- 10 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 |
|---|
| 11673-031 | UP AND UP FAMOTIDINE (FAMOTIDINE) TABLET, FILM COATED [TARGET CORPORATION] | 6 | Legacy NDC | 20250214_0d6f2ac0-295e-47ce-aedb-8cadc1e66a63.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 11673-031-65 | 11673003165 | 30 BLISTER PACK in 1 CARTON (11673-031-65) > 1 TABLET, FILM COATED in 1 BLISTER PACK | 30 blister pack | 2015-03-13 | 0000-00-00 | No | No | Current |
| 11673-031-72 | 11673003172 | 1 BOTTLE in 1 CARTON (11673-031-72) > 60 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2022-01-26 | 0000-00-00 | No | No | Current |