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 ID: 69539-006_74d56c8d-41e5-458f-8ed0-f114e061f9e5
• NDC: 69539-006
• Product Type: Human Prescription Drug
• Proprietary Name: Moxifloxacin Hydrochloride Tablets, 400 mg
• Generic Name: Moxifloxacin Hydrochloride Tablets, 400 Mg
• Dosage Form: Tablet, Film Coated
• Route of Administration: ORAL
• Marketing Start Date: 2017-09-22
• Marketing Category: ANDA / ANDA
• Application Number: ANDA208682
• Labeler Name: MSN LABORATORIES PRIVATE LIMITED
• Substance Name: MOXIFLOXACIN HYDROCHLORIDE MONOHYDRATE
• Active Ingredient Strength: 400 mg/1
• Pharm Classes: Quinolone Antimicrobial [EPC],Quinolones [CS]
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 69539-006-05

500 TABLET, FILM COATED in 1 BOTTLE (69539-006-05)

• Marketing Start Date: 2019-04-16
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 69539-006-30 [69539000630]

Moxifloxacin Hydrochloride Tablets, 400 mg TABLET, FILM COATED

• Marketing Category: ANDA
• Application Number: ANDA208682
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2019-04-16

NDC 69539-006-31 [69539000631]

Moxifloxacin Hydrochloride Tablets, 400 mg TABLET, FILM COATED

• Marketing Category: ANDA
• Application Number: ANDA208682
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2019-04-16

NDC 69539-006-11 [69539000611]

Moxifloxacin Hydrochloride Tablets, 400 mg TABLET, FILM COATED

• Marketing Category: ANDA
• Application Number: ANDA208682
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2017-09-22

NDC 69539-006-05 [69539000605]

Moxifloxacin Hydrochloride Tablets, 400 mg TABLET, FILM COATED

• Marketing Category: ANDA
• Application Number: ANDA208682
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2019-04-16

Drug Details

Active Ingredients

Ingredient	Strength
MOXIFLOXACIN HYDROCHLORIDE MONOHYDRATE	400 mg/1

OpenFDA Data

• SPL SET ID: 92305e3e-7f15-4a30-a6c9-11be6992f8e0
• Manufacturer:
  • MSN LABORATORIES PRIVATE LIMITED
• UNII:
  • B8956S8609
• 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"

NDC	Brand Name	Generic Name
69539-006	Moxifloxacin Hydrochloride Tablets, 400 mg	Moxifloxacin Hydrochloride Tablets, 400 mg
72205-001	Moxifloxacin Hydrochloride Tablets, 400 mg	Moxifloxacin Hydrochloride Tablets, 400 mg
72789-080	Moxifloxacin Hydrochloride Tablets, 400 mg	Moxifloxacin Hydrochloride Tablets, 400 mg