Ranitidine
- Product NDC
- 71713-203
- 11-digit product format
- 717130203
- Labeler code
- 71713
- Product ID
- 71713-203_676e90e4-3213-9c88-4f2b-7ce2ac795347
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ranitidine
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- Thirty Madison Inc
- Application
- ANDA078192
- Marketing category
- ANDA
- Marketing start
- 2019-05-31
- 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 |
|---|
| 71713-203 | RANITIDINE TABLET, COATED [THIRTY MADISON INC] | 3 | Legacy NDC | 20231103_8e32c53e-c13b-6061-1ae1-9f66be6185f6.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71713-203-02 | 71713020302 | 1 BOTTLE in 1 CARTON (71713-203-02) > 24 TABLET, COATED in 1 BOTTLE | 1 bottle | 2019-05-31 | 0000-00-00 | No | No | Current |
| 71713-203-05 | 71713020305 | 1 BOTTLE in 1 CARTON (71713-203-05) > 95 TABLET, COATED in 1 BOTTLE | 1 bottle | 2019-05-31 | 0000-00-00 | No | No | Current |