Acid Reducer
- Product NDC
- 69842-869
- 11-digit product format
- 698420869
- Labeler code
- 69842
- Product ID
- 69842-869_7cd094d1-2de0-6450-8245-5ee3f2de1338
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ranitidine
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- CVS HEALTH CORP
- Application
- ANDA078192
- Marketing category
- ANDA
- Marketing start
- 2010-05-01
- 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 |
|---|
| 69842-869 | ACID REDUCER (RANITIDINE) TABLET, COATED [CVS HEALTH CORP] | 2 | Legacy NDC | 20231103_91d83c64-1c69-bfd6-f881-9796551d6d92.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 69842-869-62 | 69842086962 | 1 BOTTLE in 1 CARTON (69842-869-62) > 95 TABLET, COATED in 1 BOTTLE | 1 bottle | 2010-05-01 | 0000-00-00 | No | No | Current |