Zantac
- Product NDC
- 76413-317
- 11-digit product format
- 764130317
- Labeler code
- 76413
- Product ID
- 76413-317_5a3058ab-e988-4010-99df-ee481cdd862c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ranitidine
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- Central Texas Community Health Centers
- Application
- NDA020520
- Marketing category
- NDA
- Marketing start
- 2006-12-21
- Marketing end
- 0000-00-00
- Substance
- RANITIDINE HYDROCHLORIDE
- Active strength
- 75 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 |
|---|
| 76413-317-30 | Zantac | 3 in 1 CARTON | TABLET, COATED | 3 | | 4 |
| 76413-317-30 | Zantac | 10 in 1 BLISTER PACK | TABLET, COATED | 10 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 76413-317 | ZANTAC (RANITIDINE) TABLET, COATED [CENTRAL TEXAS COMMUNITY HEALTH CENTERS] | 4 | Legacy NDC, 2 package rows | 20180427_2e846995-48b9-4062-b6f7-46884d411039.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 76413-317-30 | 76413031730 | 3 in 1 CARTON | Historical |