Ximino

Product NDC
10631-330
11-digit product format
106310330
Labeler code
10631
Product ID
10631-330_c87b3360-adb8-444e-9591-52d2b97b8e08
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
minocycline hydrochloride
Dosage form
CAPSULE, EXTENDED RELEASE
Route
ORAL
Labeler
Sun Pharmaceutical Industries, Inc
Application
NDA201922
Marketing category
NDA
Marketing start
2017-10-25
Marketing end
0000-00-00
Substance
MINOCYCLINE HYDROCHLORIDE
Active strength
45 mg/1
Pharmacologic classes
Tetracycline-class Drug [EPC],Tetracyclines [CS]
NDC exclude flag
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
10631-330-30EA - Each10631-33094983ebb-28ce-4b71-83d3-b8416ffa26ab12017-11-06