NDC 62135-626

Doxycycline Hyclate

Doxycycline Hyclate

Doxycycline Hyclate is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Chartwell Rx Llc. The primary component is Doxycycline Hyclate.

Product ID62135-626_0c6351d0-2c74-42da-883e-e145b9f7c128
NDC62135-626
Product TypeHuman Prescription Drug
Proprietary NameDoxycycline Hyclate
Generic NameDoxycycline Hyclate
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date1984-09-11
Marketing CategoryANDA / ANDA
Application NumberANDA062505
Labeler NameChartwell RX LLC
Substance NameDOXYCYCLINE HYCLATE
Active Ingredient Strength100 mg/1
Pharm ClassesTetracycline-class Drug [EPC],Tetracyclines [CS]
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 62135-626-01

100 TABLET, FILM COATED in 1 BOTTLE (62135-626-01)
Marketing Start Date2020-09-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 62135-626-09 [62135062609]

Doxycycline Hyclate TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA062505
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1984-09-11
Marketing End Date2018-10-18

NDC 62135-626-02 [62135062602]

Doxycycline Hyclate TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA062505
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1984-09-11
Marketing End Date2018-10-18

NDC 62135-626-96 [62135062696]

Doxycycline Hyclate TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA062505
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1984-09-11

NDC 62135-626-31 [62135062631]

Doxycycline Hyclate TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA062505
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1984-09-11

NDC 62135-626-06 [62135062606]

Doxycycline Hyclate TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA062505
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1984-09-11
Marketing End Date2018-10-18

NDC 62135-626-28 [62135062628]

Doxycycline Hyclate TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA062505
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1984-09-11

NDC 62135-626-10 [62135062610]

Doxycycline Hyclate TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA062505
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1984-09-11

NDC 62135-626-04 [62135062604]

Doxycycline Hyclate TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA062505
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1984-09-11
Marketing End Date2018-10-18

NDC 62135-626-03 [62135062603]

Doxycycline Hyclate TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA062505
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1984-09-11
Marketing End Date2018-10-18

NDC 62135-626-08 [62135062608]

Doxycycline Hyclate TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA062505
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1984-09-11
Marketing End Date2018-10-18

NDC 62135-626-23 [62135062623]

Doxycycline Hyclate TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA062505
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1984-09-11

NDC 62135-626-05 [62135062605]

Doxycycline Hyclate TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA062505
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date1984-09-11

NDC 62135-626-01 [62135062601]

Doxycycline Hyclate TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA062505
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1984-09-11
Marketing End Date2018-10-18

NDC 62135-626-50 [62135062650]

Doxycycline Hyclate TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA062505
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date1984-09-11

NDC 62135-626-40 [62135062640]

Doxycycline Hyclate TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA062505
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1984-09-11

NDC 62135-626-12 [62135062612]

Doxycycline Hyclate TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA062505
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1984-09-11

NDC 62135-626-20 [62135062620]

Doxycycline Hyclate TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA062505
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1984-09-11

NDC 62135-626-07 [62135062607]

Doxycycline Hyclate TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA062505
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1984-09-11
Marketing End Date2018-10-18

Drug Details

Active Ingredients

IngredientStrength
DOXYCYCLINE HYCLATE100 mg/1

OpenFDA Data

SPL SET ID:3e7cf78f-3b48-4614-9fa4-c6d1e0c05a35
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1650143

    • Pharmacological Class

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

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

    NDCBrand NameGeneric Name
    0143-3141Doxycycline HyclateDoxycycline Hyclate
    0143-3142Doxycycline HyclateDoxycycline Hyclate
    0143-9802Doxycycline HyclateDoxycycline Hyclate
    0143-9803Doxycycline HyclateDoxycycline Hyclate
    0378-0145doxycycline hyclatedoxycycline
    0378-0148doxycycline hyclatedoxycycline
    0378-0167doxycycline hyclatedoxycycline
    0378-3030Doxycycline HyclateDoxycycline Hyclate
    0378-4531Doxycycline Hyclatedoxycycline hyclate
    0378-4532Doxycycline Hyclatedoxycycline hyclate
    0378-4533Doxycycline Hyclatedoxycycline hyclate
    0378-4535Doxycycline Hyclatedoxycycline hyclate
    0440-7481Doxycycline HyclateDoxycycline Hyclate
    0440-7482Doxycycline HyclateDoxycycline Hyclate
    0463-2013Doxycycline HyclateDoxycycline Hyclate
    0463-6000Doxycycline HyclateDoxycycline Hyclate
    0527-1336Doxycycline HyclateDoxycycline Hyclate
    68047-714Doxycycline HyclateDoxycycline Hyclate
    68071-3206doxycycline hyclatedoxycycline hyclate
    68071-3243Doxycycline HyclateDoxycycline Hyclate
    68071-3252Doxycycline HyclateDoxycycline Hyclate
    68071-3104Doxycycline HyclateDoxycycline Hyclate
    68071-3386Doxycycline HyclateDoxycycline Hyclate
    68071-4478Doxycycline HyclateDoxycycline Hyclate
    68071-4354Doxycycline HyclateDoxycycline Hyclate
    68151-2022Doxycycline HyclateDoxycycline Hyclate
    68180-654doxycycline hyclatedoxycycline hyclate
    68180-653doxycycline hyclatedoxycycline hyclate
    68382-222Doxycycline hyclateDoxycycline hyclate
    68308-716Doxycycline HyclateDoxycycline Hyclate
    68308-775Doxycycline HyclateDoxycycline Hyclate
    68382-211Doxycycline hyclateDoxycycline hyclate
    68382-221Doxycycline hyclateDoxycycline hyclate
    68308-710Doxycycline HyclateDoxycycline Hyclate
    68308-715Doxycycline HyclateDoxycycline Hyclate
    68788-2112Doxycycline HyclateDoxycycline Hyclate
    68645-020Doxycycline HyclateDoxycycline Hyclate
    68788-6441Doxycycline HyclateDoxycycline Hyclate
    68788-7371Doxycycline HyclateDoxycycline Hyclate
    68788-9292Doxycycline HyclateDoxycycline Hyclate
    68788-9037Doxycycline HyclateDoxycycline Hyclate
    68788-9767Doxycycline HyclateDoxycycline Hyclate
    69097-226Doxycycline HyclateDoxycycline Hyclate
    69097-225Doxycycline HyclateDoxycycline Hyclate
    69097-227doxycycline hyclatedoxycycline hyclate
    69235-320Doxycycline HyclateDoxycycline Hyclate
    69238-1100Doxycycline HyclateDoxycycline Hyclate
    69238-1500Doxycycline HyclateDoxycycline Hyclate
    69238-1501Doxycycline HyclateDoxycycline Hyclate
    69668-515Doxycycline HyclateDoxycycline Hyclate
    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.