Acid Reducer
- Product NDC
- 68016-351
- 11-digit product format
- 680160351
- Labeler code
- 68016
- Product ID
- 68016-351_ddf34e72-a3b2-4904-910c-35c0f8f70858
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ranitidine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Premier Value
- Application
- ANDA200536
- Marketing category
- ANDA
- Marketing start
- 2012-03-30
- Marketing end
- 0000-00-00
- Substance
- RANITIDINE HYDROCHLORIDE
- Active strength
- 150 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 68016-351-24 | Acid Reducer | 24 in 1 CARTON | TABLET | 24 | | 2 |
| 68016-351-24 | Acid Reducer | 1 in 1 BLISTER PACK | TABLET | 1 | | 2 |
| 68016-351-50 | Acid Reducer | 1 in 1 CARTON | TABLET | 1 | | 2 |
| 68016-351-50 | Acid Reducer | 50 in 1 BOTTLE | TABLET | 50 | | 2 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68016-351 | ACID REDUCER (RANITIDINE) TABLET [PREMIER VALUE] | 2 | Legacy NDC, 4 package rows | 20140623_d85758e1-59bf-46e9-94f2-1a1c697c4e5d.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 68016-351-24 | 68016035124 | 24 in 1 CARTON | Historical |
| 68016-351-50 | 68016035150 | 1 in 1 CARTON | Historical |