Minocin

Product NDC
16781-403
11-digit product format
167810403
Labeler code
16781
Product ID
16781-403_bdd0be98-5e2c-4115-a434-3eced718541e
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
minocycline hydrochloride
Dosage form
CAPSULE, COATED PELLETS
Route
ORAL
Labeler
Bausch Health US, LLC
Application
NDA050649
Marketing category
NDA
Marketing start
1990-05-31
Marketing end
0000-00-00
Substance
MINOCYCLINE HYDROCHLORIDE
Active strength
100 mg/1
Pharmacologic classes
Tetracycline-class Drug [EPC],Tetracyclines [CS]
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
16781-403-50EA - Each16781-403ee5cddf6-0f56-41f8-8731-c20d8e5b91c612013-06-04
16781-403-60EA - Each16781-403c23fd09b-1cdc-403a-8cd1-b5f82e2709b512014-12-01