NDC 0440-7483

Doxycycline

Doxycycline Hyclate

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

Product ID0440-7483_a4ba92ff-e219-432b-b118-aba5737ce6b2
NDC0440-7483
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 NameLiberty Pharmaceuticals, Inc.
Substance NameDOXYCYCLINE HYCLATE
Active Ingredient Strength100 mg/1
Pharm ClassesTetracycline-class Drug [EPC],Tetracyclines [CS]
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 0440-7483-20

20 TABLET, COATED in 1 BOTTLE (0440-7483-20)
Marketing Start Date2003-07-02
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0440-7483-97 [00440748397]

Doxycycline TABLET, COATED
Marketing CategoryANDA
Application NumberANDA065095
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2003-07-02
Inactivation Date2020-01-31

NDC 0440-7483-28 [00440748328]

Doxycycline TABLET, COATED
Marketing CategoryANDA
Application NumberANDA065095
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2003-07-02
Inactivation Date2020-01-31

NDC 0440-7483-92 [00440748392]

Doxycycline TABLET, COATED
Marketing CategoryANDA
Application NumberANDA065095
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2003-07-02
Inactivation Date2020-01-31

NDC 0440-7483-20 [00440748320]

Doxycycline TABLET, COATED
Marketing CategoryANDA
Application NumberANDA065095
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2003-07-02
Inactivation Date2020-01-31

NDC 0440-7483-19 [00440748319]

Doxycycline TABLET, COATED
Marketing CategoryANDA
Application NumberANDA065095
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2003-07-02
Inactivation Date2020-01-31

NDC 0440-7483-71 [00440748371]

Doxycycline TABLET, COATED
Marketing CategoryANDA
Application NumberANDA065095
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2003-07-02
Inactivation Date2020-01-31

NDC 0440-7483-95 [00440748395]

Doxycycline TABLET, COATED
Marketing CategoryANDA
Application NumberANDA065095
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2003-07-02
Inactivation Date2020-01-31

NDC 0440-7483-14 [00440748314]

Doxycycline TABLET, COATED
Marketing CategoryANDA
Application NumberANDA065095
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2003-07-02
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
DOXYCYCLINE HYCLATE100 mg/1

OpenFDA Data

SPL SET ID:eb253341-5e11-4297-a947-5a6ece31a87b
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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