Acid Reducer
- Product NDC
- 37808-351
- 11-digit product format
- 378080351
- Labeler code
- 37808
- Product ID
- 37808-351_176a7c7c-01cc-445e-868d-3f950ac1605e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ranitidine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- H E B
- Application
- ANDA200536
- Marketing category
- ANDA
- Marketing start
- 2014-04-11
- 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 |
|---|
| 37808-351-23 | Acid Reducer | 24 in 1 BOTTLE | TABLET | 24 | | 1 |
| 37808-351-23 | Acid Reducer | 1 in 1 CARTON | TABLET | 1 | | 1 |
| 37808-351-67 | Acid Reducer | 1 in 1 CARTON | TABLET | 1 | | 1 |
| 37808-351-67 | Acid Reducer | 130 in 1 BOTTLE | TABLET | 130 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 37808-351 | ACID REDUCER (RANITIDINE) TABLET [H E B] | 1 | Legacy NDC, 4 package rows | 20140422_32536d8c-96c3-4166-a8ea-2fb4d1760303.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 37808-351-23 | 37808035123 | 24 in 1 BOTTLE | Historical |
| 37808-351-67 | 37808035167 | 1 in 1 CARTON | Historical |