members mark famotidine
- Product NDC
- 68196-061
- 11-digit product format
- 681960061
- Labeler code
- 68196
- Product ID
- 68196-061_73ae2889-f042-4b7d-9a1e-2020f813fa3b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Famotidine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Sam's West Inc
- Application
- ANDA077351
- Marketing category
- ANDA
- Marketing start
- 2006-09-28
- Marketing end
- 2022-05-31
- Substance
- FAMOTIDINE
- Active strength
- 20 mg/1
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68196-061-65 | 68196006165 | 85 TABLET in 1 BOTTLE (68196-061-65) | 85 tablet | 2006-09-28 | 2022-05-31 | No | No | Current |
| 68196-061-78 | 68196006178 | 2 BOTTLE in 1 CARTON (68196-061-78) > 50 TABLET in 1 BOTTLE | 2 bottle | 2015-07-16 | 2022-05-31 | No | No | Current |
| 68196-061-82 | 68196006182 | 2 BOTTLE in 1 CARTON (68196-061-82) > 100 TABLET in 1 BOTTLE | 2 bottle | 2006-09-28 | 2022-05-31 | No | No | Current |