acid reducer
- Product NDC
- 62011-0227
- 11-digit product format
- 620110227
- Labeler code
- 62011
- Product ID
- 62011-0227_c706df7c-3483-4f12-ac87-2e7fe39bf5e8
- 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 |
|---|
| 62011-0227-1 | acid reducer | 24 in 1 BOTTLE | TABLET | 24 | | 1 |
| 62011-0227-1 | 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 |
|---|
| 62011-0227 | ACID REDUCER (RANITIDINE ) TABLET [MCKESSON] | 1 | Legacy NDC, 2 package rows | 20140107_72445ba4-696e-44b3-b9fd-aba08fe1cba0.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 62011-0227-1 | 62011022701 | 24 in 1 BOTTLE | Historical |