Ranitidine
- Product NDC
- 68196-985
- 11-digit product format
- 681960985
- Labeler code
- 68196
- Product ID
- 68196-985_a399efc3-0b03-39b5-8763-e38cc5051d0b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ranitidine
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- Sam's West Inc
- Application
- ANDA078192
- Marketing category
- ANDA
- Marketing start
- 2011-01-05
- Marketing end
- 0000-00-00
- Substance
- RANITIDINE HYDROCHLORIDE
- Active strength
- 150 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 68196-985 | RANITIDINE TABLET, COATED [SAM'S WEST INC] | 4 | Legacy NDC | 20231103_36bd757d-f31a-b1fd-2372-fee11a264625.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68196-985-19 | 68196098519 | 2 BOTTLE in 1 CARTON (68196-985-19) > 95 TABLET, COATED in 1 BOTTLE | 2 bottle | 2011-01-05 | 0000-00-00 | No | No | Current |