Acid Reducer
- Product NDC
- 69842-871
- 11-digit product format
- 698420871
- Labeler code
- 69842
- Product ID
- 69842-871_1e2f6dad-74a0-ade7-1c23-48de03bb92b5
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ranitidine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- CVS HEALTH CORP
- Application
- ANDA075294
- Marketing category
- ANDA
- Marketing start
- 2009-07-01
- Marketing end
- 0000-00-00
- Substance
- RANITIDINE HYDROCHLORIDE
- Active strength
- 75 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 |
|---|
| 69842-871 | ACID REDUCER (RANITIDINE) TABLET [CVS HEALTH CORP] | 4 | Legacy NDC | 20231103_87ab4715-6960-237f-6e8b-24898a034909.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 69842-871-30 | 69842087130 | 1 BOTTLE in 1 CARTON (69842-871-30) > 30 TABLET in 1 BOTTLE | 1 bottle | 2013-10-01 | 0000-00-00 | No | No | Current |
| 69842-871-37 | 69842087137 | 1 BOTTLE in 1 CARTON (69842-871-37) > 160 TABLET in 1 BOTTLE | 1 bottle | 2010-03-01 | 0000-00-00 | No | No | Current |
| 69842-871-80 | 69842087180 | 1 BOTTLE in 1 CARTON (69842-871-80) > 80 TABLET in 1 BOTTLE | 1 bottle | 2009-07-01 | 0000-00-00 | No | No | Current |