RANITIDINE
- Product NDC
- 51655-681
- 11-digit product format
- 516550681
- Labeler code
- 51655
- Product ID
- 51655-681_ed1c2498-b8dd-4708-b009-0c928f534f53
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ranitidine hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Northwind Pharmaceuticals, LLC
- Application
- ANDA077824
- Marketing category
- ANDA
- Marketing start
- 2014-09-15
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51655-681 | RANITIDINE (RANITIDINE HYDROCHLORIDE) TABLET [NORTHWIND PHARMACEUTICALS, LLC] | 2 | Legacy NDC | 20141110_fd4d06b3-8fd9-49f4-9dcb-0a57386fe4de.zip |