Doxycycline Hyclate

Product NDC
50090-6133
11-digit product format
500906133
Labeler code
50090
Product ID
50090-6133_72e80edd-b0d6-4b10-9b79-ffd12490a591
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Doxycycline Hyclate
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA062269
Marketing category
ANDA
Marketing start
2016-10-01
Substance
DOXYCYCLINE HYCLATE
Active strength
100 mg/1
Pharmacologic classes
Tetracycline-class Drug [EPC], Tetracyclines [CS]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Doxycycline Hyclate
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
DOXYCYCLINE HYCLATE100 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
Unii19XTS3T51U
Rxcui1650143

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
50090-6133-05009061330010 TABLET, FILM COATED in 1 BOTTLE (50090-6133-0) 2022-10-030000-00-00NoNoCurrent
50090-6133-15009061330114 TABLET, FILM COATED in 1 BOTTLE (50090-6133-1) 2022-10-030000-00-00NoNoCurrent
50090-6133-35009061330320 TABLET, FILM COATED in 1 BOTTLE (50090-6133-3) 2022-10-030000-00-00NoNoCurrent
50090-6133-55009061330528 TABLET, FILM COATED in 1 BOTTLE (50090-6133-5) 2022-10-030000-00-00NoNoCurrent
50090-6133-65009061330630 TABLET, FILM COATED in 1 BOTTLE (50090-6133-6) 2022-10-030000-00-00NoNoCurrent
50090-6133-85009061330860 TABLET, FILM COATED in 1 BOTTLE (50090-6133-8) 2022-10-030000-00-00NoNoCurrent