NDC 68999-417

doxycycline

Doxycycline

doxycycline is a Oral Powder, For Suspension in the Human Prescription Drug category. It is labeled and distributed by Chartwell Governmental & Specialty Rx, Llc. The primary component is Doxycycline.

Product ID68999-417_d0e9386e-bb36-15c7-e053-2a95a90ab5a1
NDC68999-417
Product TypeHuman Prescription Drug
Proprietary Namedoxycycline
Generic NameDoxycycline
Dosage FormPowder, For Suspension
Route of AdministrationORAL
Marketing Start Date2008-07-16
Marketing CategoryANDA /
Application NumberANDA065454
Labeler NameChartwell Governmental & Specialty RX, LLC
Substance NameDOXYCYCLINE
Active Ingredient Strength25 mg/5mL
Pharm ClassesTetracycline-class Drug [EPC],Tetracyclines [CS]
NDC Exclude FlagN
Listing Certified Through2022-12-31

Packaging

NDC 68999-417-46

60 mL in 1 BOTTLE, GLASS (68999-417-46)
Marketing Start Date2021-09-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 68999-417-01 [68999041701]

Doxycycline POWDER, FOR SUSPENSION
Marketing CategoryANDA
Application NumberANDA065454
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2008-07-16
Marketing End Date2008-07-16

Drug Details

NDC Crossover Matching brand name "doxycycline" or generic name "Doxycycline"

NDCBrand NameGeneric Name
0115-1327DoxycyclineDoxycycline
0143-2112DoxycyclineDoxycycline hyclate
0143-9381DoxycyclineDoxycycline
0179-0129DoxycyclineDoxycycline
0378-5475Doxycyclinedoxycycline
0378-6021DoxycyclineDoxycycline
0378-6022DoxycyclineDoxycycline
0378-6023DoxycyclineDoxycycline
0378-6124DoxycyclineDoxycycline
0404-9855DOXYCYCLINEdoxycycline
0440-7483DoxycyclineDoxycycline hyclate
0527-1335DoxycyclineDoxycycline
0527-1338DoxycyclineDoxycycline
68071-4110DoxycyclineDoxycycline
68084-743DoxycyclineDoxycycline
68180-650DOXYCYCLINEDOXYCYCLINE
68180-657DOXYCYCLINEDOXYCYCLINE
68180-652DOXYCYCLINEDOXYCYCLINE
68180-651DOXYCYCLINEDOXYCYCLINE
68382-706doxycyclinedoxycycline
68382-910DoxycyclineDoxycycline
68382-707doxycyclinedoxycycline
68382-782doxycyclinedoxycycline
68382-911DoxycyclineDoxycycline
68387-381DoxycyclineDoxycycline
68645-021DoxycyclineDoxycycline
0527-1537DoxycyclineDoxycycline
69007-822DOXYCYCLINEDOXYCYCLINE
0527-1535DoxycyclineDoxycycline
69097-228DoxycyclineDoxycycline
70518-0038DoxycyclineDoxycycline
70518-0221DoxycyclineDoxycycline
70518-0187DoxycyclineDoxycycline
70518-0213DOXYCYCLINEDOXYCYCLINE
70710-1124DoxycyclineDoxycycline
70710-1121DoxycyclineDoxycycline
70710-1123DoxycyclineDoxycycline
70771-1006DoxycyclineDoxycycline
70710-1122DoxycyclineDoxycycline
70771-1008DoxycyclineDoxycycline
70771-1007DoxycyclineDoxycycline
70771-1009DoxycyclineDoxycycline
70771-1122DoxycyclineDoxycycline
70771-1121DoxycyclineDoxycycline
70934-178DoxycyclineDoxycycline
71205-135DoxycyclineDoxycycline
71335-0168DoxycyclineDoxycycline
71335-0436doxycyclinedoxycycline
71335-0823DoxycyclineDoxycycline
71610-130DoxycyclineDoxycycline

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.