NDC 68071-4110

Doxycycline

Doxycycline Hyclate

Doxycycline is a Oral Tablet, Coated in the Human Prescription Drug category. It is labeled and distributed by Nucare Pharmaceuticals,inc.. The primary component is Doxycycline Hyclate.

Product ID68071-4110_5abd662a-51e2-8a78-e053-2a91aa0ae06f
NDC68071-4110
Product TypeHuman Prescription Drug
Proprietary NameDoxycycline
Generic NameDoxycycline Hyclate
Dosage FormTablet, Coated
Route of AdministrationORAL
Marketing Start Date2003-07-02
Marketing CategoryANDA / ANDA
Application NumberANDA065095
Labeler NameNuCare Pharmaceuticals,Inc.
Substance NameDOXYCYCLINE HYCLATE
Active Ingredient Strength100 mg/1
Pharm ClassesTetracycline-class Drug [EPC],Tetracyclines [CS]
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 68071-4110-2

20 TABLET, COATED in 1 BOTTLE (68071-4110-2)
Marketing Start Date2017-10-04
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 68071-4110-4 [68071411004]

Doxycycline TABLET, COATED
Marketing CategoryANDA
Application NumberANDA065095
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-10-04
Marketing End Date2019-12-31
Inactivation Date2020-01-31

NDC 68071-4110-1 [68071411001]

Doxycycline TABLET, COATED
Marketing CategoryANDA
Application NumberANDA065095
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-10-04
Marketing End Date2019-12-31
Inactivation Date2020-01-31

NDC 68071-4110-5 [68071411005]

Doxycycline TABLET, COATED
Marketing CategoryANDA
Application NumberANDA065095
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-10-04
Marketing End Date2019-12-31
Inactivation Date2020-01-31

NDC 68071-4110-7 [68071411007]

Doxycycline TABLET, COATED
Marketing CategoryANDA
Application NumberANDA065095
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-10-04
Marketing End Date2019-12-31
Inactivation Date2020-01-31

NDC 68071-4110-3 [68071411003]

Doxycycline TABLET, COATED
Marketing CategoryANDA
Application NumberANDA065095
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-10-04
Marketing End Date2019-12-31
Inactivation Date2020-01-31

NDC 68071-4110-2 [68071411002]

Doxycycline TABLET, COATED
Marketing CategoryANDA
Application NumberANDA065095
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-10-04
Marketing End Date2019-12-31
Inactivation Date2020-01-31

NDC 68071-4110-6 [68071411006]

Doxycycline TABLET, COATED
Marketing CategoryANDA
Application NumberANDA065095
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-10-04
Marketing End Date2019-12-31
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
DOXYCYCLINE HYCLATE100 mg/1

OpenFDA Data

SPL SET ID:5abd662a-51e1-8a78-e053-2a91aa0ae06f
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1650143

    • Pharmacological Class

    • Tetracycline-class Drug [EPC]
    • Tetracyclines [CS]

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

    NDCBrand NameGeneric Name
    0115-1327DoxycyclineDoxycycline
    0143-2112DoxycyclineDoxycycline hyclate
    0143-9381DoxycyclineDoxycycline
    0179-0129DoxycyclineDoxycycline
    68071-4110DoxycyclineDoxycycline
    68084-743DoxycyclineDoxycycline
    0440-7483DoxycyclineDoxycycline
    68180-650DOXYCYCLINEDOXYCYCLINE
    68180-657DOXYCYCLINEDOXYCYCLINE
    68180-652DOXYCYCLINEDOXYCYCLINE
    68180-651DOXYCYCLINEDOXYCYCLINE
    68382-706doxycyclinedoxycycline
    68382-910DoxycyclineDoxycycline
    68382-707doxycyclinedoxycycline
    68382-782doxycyclinedoxycycline
    68382-911DoxycyclineDoxycycline
    68387-381DoxycyclineDoxycycline
    68645-021DoxycyclineDoxycycline
    0527-1338DoxycyclineDoxycycline
    0527-1335DoxycyclineDoxycycline
    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
    76519-1134DOXYCYCLINEDOXYCYCLINE
    76519-1206DOXYCYCLINEDOXYCYCLINE
    0713-0428DoxycyclineDoxycycline
    0713-0427DoxycyclineDoxycycline
    0713-0429DoxycyclineDoxycycline
    0713-0555DoxycyclineDoxycycline
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