Ranitidine
- Product NDC
- 49999-043
- 11-digit product format
- 499990043
- Labeler code
- 49999
- Product ID
- 49999-043_c6f57c41-4e94-4774-be6d-42feaf96d843
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ranitidine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Quality Care Products, LLC
- Application
- ANDA078542
- Marketing category
- ANDA
- Marketing start
- 2008-11-19
- Marketing end
- 2022-05-31
- 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
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 49999-043-30 | 49999004330 | 30 TABLET, FILM COATED in 1 BOTTLE (49999-043-30) | 2008-11-19 | 2022-05-31 | No | No | Current |
| 49999-043-60 | 49999004360 | 60 TABLET, FILM COATED in 1 BOTTLE (49999-043-60) | 2008-11-19 | 2022-05-31 | No | No | Current |
| 49999-043-90 | 49999004390 | 90 TABLET, FILM COATED in 1 BOTTLE (49999-043-90) | 2008-11-19 | 2022-05-31 | No | No | Current |