NDC 69539-006

Moxifloxacin Hydrochloride Tablets, 400 mg

Moxifloxacin Hydrochloride Tablets, 400 Mg

Moxifloxacin Hydrochloride Tablets, 400 mg is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Msn Laboratories Private Limited. The primary component is Moxifloxacin Hydrochloride Monohydrate.

Product ID69539-006_74d56c8d-41e5-458f-8ed0-f114e061f9e5
NDC69539-006
Product TypeHuman Prescription Drug
Proprietary NameMoxifloxacin Hydrochloride Tablets, 400 mg
Generic NameMoxifloxacin Hydrochloride Tablets, 400 Mg
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2017-09-22
Marketing CategoryANDA / ANDA
Application NumberANDA208682
Labeler NameMSN LABORATORIES PRIVATE LIMITED
Substance NameMOXIFLOXACIN HYDROCHLORIDE MONOHYDRATE
Active Ingredient Strength400 mg/1
Pharm ClassesQuinolone Antimicrobial [EPC],Quinolones [CS]
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 69539-006-05

500 TABLET, FILM COATED in 1 BOTTLE (69539-006-05)
Marketing Start Date2019-04-16
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 69539-006-30 [69539000630]

Moxifloxacin Hydrochloride Tablets, 400 mg TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA208682
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-04-16

NDC 69539-006-31 [69539000631]

Moxifloxacin Hydrochloride Tablets, 400 mg TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA208682
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-04-16

NDC 69539-006-11 [69539000611]

Moxifloxacin Hydrochloride Tablets, 400 mg TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA208682
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-09-22

NDC 69539-006-05 [69539000605]

Moxifloxacin Hydrochloride Tablets, 400 mg TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA208682
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-04-16

Drug Details

Active Ingredients

IngredientStrength
MOXIFLOXACIN HYDROCHLORIDE MONOHYDRATE400 mg/1

OpenFDA Data

SPL SET ID:92305e3e-7f15-4a30-a6c9-11be6992f8e0
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 311787
  • UPC Code
  • 0369539006311
  • 0369539006052
  • Pharmacological Class

    • Quinolone Antimicrobial [EPC]
    • Quinolones [CS]

    NDC Crossover Matching brand name "Moxifloxacin Hydrochloride Tablets, 400 mg" or generic name "Moxifloxacin Hydrochloride Tablets, 400 Mg"

    NDCBrand NameGeneric Name
    69539-006Moxifloxacin Hydrochloride Tablets, 400 mgMoxifloxacin Hydrochloride Tablets, 400 mg
    72205-001Moxifloxacin Hydrochloride Tablets, 400 mgMoxifloxacin Hydrochloride Tablets, 400 mg
    72789-080Moxifloxacin Hydrochloride Tablets, 400 mgMoxifloxacin Hydrochloride Tablets, 400 mg

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