Ranitidine
- Product NDC
- 0904-6921
- 11-digit product format
- 009046921
- Labeler code
- 0904
- Product ID
- 0904-6921_2a917fc5-06a6-d0e3-f8d4-39013116a446
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ranitidine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- MAJOR PHARMACEUTICALS
- Application
- ANDA075294
- Marketing category
- ANDA
- Marketing start
- 2019-05-28
- Marketing end
- 0000-00-00
- Substance
- RANITIDINE HYDROCHLORIDE
- Active strength
- 75 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0904-6921-46 | 00904692146 | 1 BOTTLE in 1 CARTON (0904-6921-46) > 30 TABLET in 1 BOTTLE | 1 bottle | 2019-05-28 | 0000-00-00 | No | No | Current |
| 0904-6921-52 | 00904692152 | 1 BOTTLE in 1 CARTON (0904-6921-52) > 60 TABLET in 1 BOTTLE | 1 bottle | 2019-05-28 | 0000-00-00 | No | No | Current |