NDC 70771-1167

minocycline hydrochloride

Minocycline Hydrochloride

minocycline hydrochloride is a Oral Tablet, Extended Release in the Human Prescription Drug category. It is labeled and distributed by Cadila Healthcare Limited. The primary component is Minocycline Hydrochloride.

Product ID70771-1167_501b1d9e-de62-4f0c-9233-fa7af6df2057
NDC70771-1167
Product TypeHuman Prescription Drug
Proprietary Nameminocycline hydrochloride
Generic NameMinocycline Hydrochloride
Dosage FormTablet, Extended Release
Route of AdministrationORAL
Marketing Start Date2018-03-07
Marketing CategoryANDA / ANDA
Application NumberANDA203553
Labeler NameCadila Healthcare Limited
Substance NameMINOCYCLINE HYDROCHLORIDE
Active Ingredient Strength135 mg/1
Pharm ClassesTetracycline-class Drug [EPC],Tetracyclines [CS]
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 70771-1167-0

1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1167-0)
Marketing Start Date2018-03-07
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 70771-1167-9 [70771116709]

minocycline hydrochloride TABLET, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA203553
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2018-03-07

NDC 70771-1167-7 [70771116707]

minocycline hydrochloride TABLET, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA203553
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2018-03-07

NDC 70771-1167-5 [70771116705]

minocycline hydrochloride TABLET, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA203553
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2018-03-07

NDC 70771-1167-3 [70771116703]

minocycline hydrochloride TABLET, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA203553
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2018-03-07

NDC 70771-1167-1 [70771116701]

minocycline hydrochloride TABLET, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA203553
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2018-03-07

NDC 70771-1167-0 [70771116700]

minocycline hydrochloride TABLET, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA203553
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2018-03-07

Drug Details

Active Ingredients

IngredientStrength
MINOCYCLINE HYDROCHLORIDE135 mg/1

OpenFDA Data

SPL SET ID:8bf9cf23-8ffc-401f-981d-4878d694a468
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1013665
  • 629695
  • 629697
  • 629699
  • 1013659
  • UPC Code
  • 0370771115617
  • 0370771115716
  • 0370771116713
  • 0370771115518
  • Pharmacological Class

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

    NDC Crossover Matching brand name "minocycline hydrochloride" or generic name "Minocycline Hydrochloride"

    NDCBrand NameGeneric Name
    0093-2133Minocycline HydrochlorideMinocycline Hydrochloride
    0093-2134Minocycline HydrochlorideMinocycline Hydrochloride
    0093-7741Minocycline HydrochlorideMinocycline Hydrochloride
    0093-7742Minocycline HydrochlorideMinocycline Hydrochloride
    0093-7743Minocycline HydrochlorideMinocycline Hydrochloride
    0115-9935minocycline hydrochlorideminocycline hydrochloride
    0115-9936minocycline hydrochlorideminocycline hydrochloride
    0378-4293Minocycline Hydrochlorideminocycline hydrochloride
    0378-4294Minocycline Hydrochlorideminocycline hydrochloride
    0440-7805Minocycline hydrochlorideMinocycline hydrochloride
    0591-3153Minocycline HydrochlorideMinocycline Hydrochloride
    0591-5694Minocycline HydrochlorideMinocycline Hydrochloride
    0591-5695Minocycline HydrochlorideMinocycline Hydrochloride
    0781-5385Minocycline HydrochlorideMinocycline Hydrochloride
    0781-5386Minocycline HydrochlorideMinocycline Hydrochloride
    0781-5387Minocycline HydrochlorideMinocycline Hydrochloride
    0904-6888Minocycline HydrochlorideMinocycline Hydrochloride
    13668-482Minocycline HydrochlorideMinocycline Hydrochloride
    67877-438Minocycline HydrochlorideMinocycline Hydrochloride
    67877-576Minocycline HydrochlorideMinocycline Hydrochloride
    67877-578Minocycline HydrochlorideMinocycline Hydrochloride
    67877-437Minocycline HydrochlorideMinocycline Hydrochloride
    67877-643Minocycline HydrochlorideMinocycline Hydrochloride
    67877-644Minocycline HydrochlorideMinocycline Hydrochloride
    67877-577Minocycline HydrochlorideMinocycline Hydrochloride
    68071-1937Minocycline HydrochlorideMinocycline Hydrochloride
    68071-3338Minocycline HydrochlorideMinocycline Hydrochloride
    68071-3307Minocycline HydrochlorideMinocycline Hydrochloride
    68071-4227Minocycline HydrochlorideMinocycline Hydrochloride
    68071-4163Minocycline HydrochlorideMinocycline Hydrochloride
    68071-4216Minocycline HydrochlorideMinocycline Hydrochloride
    68151-2299Minocycline HydrochlorideMinocycline Hydrochloride
    68180-381Minocycline HydrochlorideMinocycline Hydrochloride
    68180-380Minocycline HydrochlorideMinocycline Hydrochloride
    68180-379Minocycline HydrochlorideMinocycline Hydrochloride
    68180-460Minocycline HydrochlorideMinocycline Hydrochloride
    68382-535minocycline hydrochlorideminocycline hydrochloride
    68382-531minocycline hydrochlorideminocycline hydrochloride
    68382-316Minocycline hydrochlorideMinocycline hydrochloride
    68382-318Minocycline hydrochlorideMinocycline hydrochloride
    68382-533minocycline hydrochlorideminocycline hydrochloride
    68382-551minocycline hydrochlorideminocycline hydrochloride
    68382-317Minocycline hydrochlorideMinocycline hydrochloride
    68382-552minocycline hydrochlorideminocycline hydrochloride
    68682-467minocycline hydrochlorideminocycline hydrochloride
    68682-466minocycline hydrochlorideminocycline hydrochloride
    68682-468minocycline hydrochlorideminocycline hydrochloride
    68788-9085Minocycline hydrochlorideMinocycline hydrochloride
    68788-6997Minocycline HydrochlorideMinocycline Hydrochloride
    68788-7052Minocycline HydrochlorideMinocycline Hydrochloride

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