Clindamycin hydrochloride
- Product NDC
- 51655-530
- 11-digit product format
- 516550530
- Labeler code
- 51655
- Product ID
- 51655-530_0af35e27-d4d7-4fed-9a51-8bd35bfe839e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clindamycin hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Northwind Pharmaceuticals
- Application
- ANDA065442
- Marketing category
- ANDA
- Marketing start
- 2014-06-01
- Marketing end
- 0000-00-00
- Substance
- CLINDAMYCIN HYDROCHLORIDE
- Active strength
- 300 mg/1
- Pharmacologic classes
- Decreased Sebaceous Gland Activity [PE],Lincosamide Antibacterial [EPC],Lincosamides [CS]
- 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 |
|---|
| 51655-530 | CLINDAMYCIN HYDROCHLORIDE CAPSULE [NORTHWIND PHARMACEUTICALS] | 2 | Legacy NDC | 20140618_ac36ddf8-a9d7-4f62-9703-57a7a7627512.zip |