Ranitidine
- Product NDC
- 11673-849
- 11-digit product format
- 116730849
- Labeler code
- 11673
- Product ID
- 11673-849_a83ae8ad-53af-194a-d54d-a42ec5d69de4
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ranitidine
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- Target Corporation
- Application
- ANDA078192
- Marketing category
- ANDA
- Marketing start
- 2019-03-15
- Marketing end
- 0000-00-00
- Substance
- RANITIDINE HYDROCHLORIDE
- Active strength
- 150 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 11673-849 | RANITIDINE TABLET, COATED [TARGET CORPORATION] | 2 | Legacy NDC | 20231103_6f9c004b-447a-dbd3-4108-338a9e87fff1.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 11673-849-40 | 11673084940 | 1 BOTTLE in 1 CARTON (11673-849-40) > 40 TABLET, COATED in 1 BOTTLE | 1 bottle | 2019-03-15 | 0000-00-00 | No | No | Current |