Ranitidine
- Product NDC
- 63868-480
- 11-digit product format
- 638680480
- Labeler code
- 63868
- Product ID
- 63868-480_c7ef3af9-9b7c-fc68-c47c-2676a68e7147
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ranitidine
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- Chain Drug Marketing Association
- Application
- ANDA078192
- Marketing category
- ANDA
- Marketing start
- 2018-07-01
- 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 |
|---|
| 63868-480 | RANITIDINE TABLET, COATED [CHAIN DRUG MARKETING ASSOCIATION] | 2 | Legacy NDC | 20231103_7dc77beb-15c0-3543-f30d-7af8408e0dae.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63868-480-24 | 63868048024 | 1 BOTTLE in 1 CARTON (63868-480-24) > 24 TABLET, COATED in 1 BOTTLE | 1 bottle | 2018-07-01 | 0000-00-00 | No | No | Current |
| 63868-480-50 | 63868048050 | 1 BOTTLE in 1 CARTON (63868-480-50) > 50 TABLET, COATED in 1 BOTTLE | 1 bottle | 2018-07-01 | 0000-00-00 | No | No | Current |