Ranitidine
- Product NDC
- 63629-8236
- 11-digit product format
- 636298236
- Labeler code
- 63629
- Product ID
- 63629-8236_dd505d62-58c5-4f3b-aa28-a75e71913ab0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ranitidine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA077824
- Marketing category
- ANDA
- Marketing start
- 2009-12-16
- Marketing end
- 0000-00-00
- Substance
- RANITIDINE HYDROCHLORIDE
- Active strength
- 150 mg/1
- Pharmacologic classes
- Histamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 63629-8236-1 | 63629823601 | 30 TABLET in 1 BOTTLE (63629-8236-1) | 30 tablet | 2019-09-06 | 0000-00-00 | No | No | Current |
| 63629-8236-2 | 63629823602 | 60 TABLET in 1 BOTTLE (63629-8236-2) | 60 tablet | 2019-09-06 | 0000-00-00 | No | No | Current |
| 63629-8236-3 | 63629823603 | 90 TABLET in 1 BOTTLE (63629-8236-3) | 90 tablet | 2019-09-06 | 0000-00-00 | No | No | Current |