up and up famotidine
- Product NDC
- 11673-414
- 11-digit product format
- 116730414
- Labeler code
- 11673
- Product ID
- 11673-414_4ab1b57d-0782-4882-a144-3c96cfe05fad
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- famotidine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Target Corporation
- Application
- ANDA077351
- Marketing category
- ANDA
- Marketing start
- 2022-01-25
- 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 |
|---|
| 11673-414 | UP AND UP FAMOTIDINE (FAMOTIDINE) TABLET, FILM COATED [TARGET CORPORATION] | 2 | Legacy NDC | 20220311_cde17ba0-690e-4d14-9d0a-677a8f91d79e.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 11673-414-63 | 11673041463 | 1 BOTTLE in 1 CARTON (11673-414-63) > 25 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2022-01-25 | 0000-00-00 | No | No | Current |