acid reducer
- Product NDC
- 49348-026
- 11-digit product format
- 493480026
- Labeler code
- 49348
- Product ID
- 49348-026_cc539679-b068-4d74-a885-b3801b84c5e6
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ranitidine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- McKesson
- Application
- ANDA200536
- Marketing category
- ANDA
- Marketing start
- 2014-01-07
- 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 |
|---|
| 49348-026-04 | acid reducer | 1 in 1 CARTON | TABLET | 1 | | 1 |
| 49348-026-04 | acid reducer | 24 in 1 BOTTLE | TABLET | 24 | | 1 |
| 49348-026-54 | acid reducer | 65 in 1 BOTTLE | TABLET | 65 | | 1 |
| 49348-026-54 | acid reducer | 1 in 1 CARTON | TABLET | 1 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 49348-026 | ACID REDUCER (RANITIDINE) TABLET [MCKESSON] | 1 | Legacy NDC, 4 package rows | 20140107_f2d98424-bbfe-4d50-82fe-1dec283ae819.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 49348-026-04 | 49348002604 | 1 in 1 CARTON | Historical |
| 49348-026-54 | 49348002654 | 65 in 1 BOTTLE | Historical |