Doxycycline hyclate

Product NDC
68382-221
11-digit product format
683820221
Labeler code
68382
Product ID
68382-221_504488d3-8e11-42ce-bce7-ede2307db721
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Doxycycline hyclate
Dosage form
CAPSULE
Route
ORAL
Labeler
Zydus Pharmaceuticals (USA) Inc.
Application
ANDA207774
Marketing category
ANDA
Marketing start
2018-09-12
Marketing end
0000-00-00
Substance
DOXYCYCLINE HYCLATE
Active strength
50 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

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
68382-221-0168382022101100 CAPSULE in 1 BOTTLE (68382-221-01) 100 capsule2018-09-120000-00-00NoNoCurrent
68382-221-0568382022105500 CAPSULE in 1 BOTTLE (68382-221-05) 500 capsule2018-09-120000-00-00NoNoCurrent
68382-221-10683820221101000 CAPSULE in 1 BOTTLE (68382-221-10) 1000 capsule2018-09-120000-00-00NoNoCurrent
68382-221-186838202211850 CAPSULE in 1 BOTTLE (68382-221-18) 50 capsule2018-09-120000-00-00NoNoCurrent
68382-221-776838202217710 BLISTER PACK in 1 CARTON (68382-221-77) > 10 CAPSULE in 1 BLISTER PACK (68382-221-30) 10 blister pack2018-09-120000-00-00NoNoCurrent