NDC 53002-0670

Doxycycline

Doxycycline

Doxycycline is a Oral Capsule in the Human Prescription Drug category. It is labeled and distributed by Rpk Pharmaceuticals, Inc.. The primary component is Doxycycline.

Product ID53002-0670_069b3df0-3a36-48c2-a577-a02fb4addb65
NDC53002-0670
Product TypeHuman Prescription Drug
Proprietary NameDoxycycline
Generic NameDoxycycline
Dosage FormCapsule
Route of AdministrationORAL
Marketing Start Date2016-04-29
Marketing CategoryANDA / ANDA
Application NumberANDA204446
Labeler NameRPK Pharmaceuticals, Inc.
Substance NameDOXYCYCLINE
Active Ingredient Strength100 mg/1
Pharm ClassesTetracycline-class Drug [EPC],Tetracyclines [CS]
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 53002-0670-1

2 CAPSULE in 1 BOTTLE (53002-0670-1)
Marketing Start Date2017-10-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 53002-0670-2 [53002067002]

Doxycycline CAPSULE
Marketing CategoryANDA
Application NumberANDA204446
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-10-01
Inactivation Date2020-01-31

NDC 53002-0670-6 [53002067006]

Doxycycline CAPSULE
Marketing CategoryANDA
Application NumberANDA204446
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-10-01
Inactivation Date2020-01-31

NDC 53002-0670-4 [53002067004]

Doxycycline CAPSULE
Marketing CategoryANDA
Application NumberANDA204446
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-10-01
Inactivation Date2020-01-31

NDC 53002-0670-1 [53002067001]

Doxycycline CAPSULE
Marketing CategoryANDA
Application NumberANDA204446
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-10-01
Inactivation Date2020-01-31

NDC 53002-0670-7 [53002067007]

Doxycycline CAPSULE
Marketing CategoryANDA
Application NumberANDA204446
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-10-01
Inactivation Date2020-01-31

NDC 53002-0670-3 [53002067003]

Doxycycline CAPSULE
Marketing CategoryANDA
Application NumberANDA204446
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-10-01
Inactivation Date2020-01-31

NDC 53002-0670-9 [53002067009]

Doxycycline CAPSULE
Marketing CategoryANDA
Application NumberANDA204446
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-10-01
Inactivation Date2020-01-31

NDC 53002-0670-5 [53002067005]

Doxycycline CAPSULE
Marketing CategoryANDA
Application NumberANDA204446
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-10-01
Inactivation Date2020-01-31

NDC 53002-0670-0 [53002067000]

Doxycycline CAPSULE
Marketing CategoryANDA
Application NumberANDA204446
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-10-01
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
DOXYCYCLINE100 mg/1

OpenFDA Data

SPL SET ID:1aad420b-a9f3-414e-bff3-787d8941aae7
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1649990
  • PHarm Class EPC
  • Tetracycline-class Drug [EPC]
  • NUI Code
  • N0000007948
  • N0000175882
  • Pharmacological Class

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

    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

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