Ranitidine
- Product NDC
- 43598-808
- 11-digit product format
- 435980808
- Labeler code
- 43598
- Product ID
- 43598-808_fcc59e60-096c-b6bf-f6a4-d95326fb63d2
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ranitidine
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- Dr. Reddy's Laboratories Inc.
- Application
- ANDA078192
- Marketing category
- ANDA
- Marketing start
- 2018-12-26
- 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 |
|---|
| 43598-808 | RANITIDINE TABLET, COATED [DR. REDDY'S LABORATORIES INC.] | 2 | Legacy NDC | 20231103_2c14e69d-b4ac-4342-c433-ef0946f980be.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 43598-808-62 | 43598080862 | 1 BOTTLE in 1 CARTON (43598-808-62) > 95 TABLET, COATED in 1 BOTTLE | 1 bottle | 2018-12-26 | 0000-00-00 | No | No | Current |
| 43598-808-65 | 43598080865 | 1 BOTTLE in 1 CARTON (43598-808-65) > 220 TABLET, COATED in 1 BOTTLE | 1 bottle | 2018-12-26 | 0000-00-00 | No | No | Current |