Moxifloxacin Hydrochloride Tablets, 400 mg is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Novadoz Pharmaceuticals Llc. The primary component is Moxifloxacin Hydrochloride Monohydrate.
Product ID | 72205-001_79a88ea4-ddf4-4ee9-acc2-91047ce636d5 |
NDC | 72205-001 |
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 | 2018-07-21 |
Marketing Category | ANDA / ANDA |
Application Number | ANDA208682 |
Labeler Name | Novadoz Pharmaceuticals LLC |
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 |
Marketing Start Date | 2019-04-16 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | ANDA |
Application Number | ANDA208682 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2019-04-16 |
Marketing Category | ANDA |
Application Number | ANDA208682 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2019-04-16 |
Marketing Category | ANDA |
Application Number | ANDA208682 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2019-04-16 |
Marketing Category | ANDA |
Application Number | ANDA208682 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2018-07-21 |
Ingredient | Strength |
---|---|
MOXIFLOXACIN HYDROCHLORIDE MONOHYDRATE | 400 mg/1 |
SPL SET ID: | 04e0936f-2248-48e4-8031-ac6ccc2df294 |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI | |
UPC Code |
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 |