Ranitidine
- Product NDC
- 68071-2190
- 11-digit product format
- 680712190
- Labeler code
- 68071
- Product ID
- 68071-2190_bc092284-3583-55ee-e053-2a95a90ae33a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ranitidine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals, Inc.
- 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
- 2022-12-31
- 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 |
|---|
| 68071-2190-3 | 68071219003 | 30 TABLET in 1 BOTTLE (68071-2190-3) | 30 tablet | 2017-06-09 | 0000-00-00 | No | No | Current |
| 68071-2190-4 | 68071219004 | 40 TABLET in 1 BOTTLE (68071-2190-4) | 40 tablet | 2017-06-09 | 0000-00-00 | No | No | Current |
| 68071-2190-6 | 68071219006 | 60 TABLET in 1 BOTTLE (68071-2190-6) | 60 tablet | 2017-06-09 | 0000-00-00 | No | No | Current |
| 68071-2190-8 | 68071219008 | 180 TABLET in 1 BOTTLE (68071-2190-8) | 180 tablet | 2017-06-09 | 0000-00-00 | No | No | Current |
| 68071-2190-9 | 68071219009 | 90 TABLET in 1 BOTTLE (68071-2190-9) | 90 tablet | 2017-06-09 | 0000-00-00 | No | No | Current |