Ranitidine 150
- Product NDC
- 68998-397
- 11-digit product format
- 689980397
- Labeler code
- 68998
- Product ID
- 68998-397_0d136b75-d474-492c-bc8f-737fa3d31592
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ranitidine HCl Tablets 150mg
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- Marc Glassman, Inc.
- Application
- ANDA078192
- Marketing category
- ANDA
- Marketing start
- 2018-10-01
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68998-397-93 | 68998039793 | 2 BLISTER PACK in 1 CARTON (68998-397-93) > 12 TABLET, COATED in 1 BLISTER PACK | 2 blister pack | 2018-10-01 | 0000-00-00 | No | No | Current |