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| Number of Labels Found: 381 of 27052 current-in-use and prior versions. (To refine your search and narrow your results, click here.) |
| Your Search: All labels beginning with the letter "Z" |
Brand Name
(Generic) |
Sponsor | Latest Ver. # Published |
Dosage Forms | Category Appl./Mono. No. |
Product Type | |||||||||
| 2 | ACCOLATE (Zafirlukast) | AstraZeneca Pharmaceuticals LP | * | Ver: 2 (R3) Jan 05, 2007 |
Tablet, Film Coated | | Human Prescription Drug Labeling | |||||||
| 1 | ACCOLATE (Zafirlukast) | AstraZeneca Pharmaceuticals LP | * | Ver: 7 (R4) Aug 06, 2010 |
Tablet, Film Coated | NDA NDA020547 | Human Prescription Drug Label | |||||||
| 3 | ACCOLATE (Zafirlukast) | State of Florida DOH Central Pharmacy | Ver: 1 (R4) Aug 06, 2010 |
Tablet, Film Coated | NDA NDA020547 | Human Prescription Drug Label | ||||||||
| 4 | Alba Kids Mineral Sunblock SPF 30 (Zinc Oxide, Titanium Dioxide) | The Hain Celestial Group, Inc. | Ver: 1 (R4) Jul 02, 2010 |
Cream | OTC monograph not final part352 | Human OTC Drug Label | ||||||||
| 5 | Alba Sunblock Facial SPF 20 (Zinc Oxide, Titanium Dioxide) | The Hain Celestial Group, Inc. | Ver: 1 (R4) Jul 01, 2010 |
Cream | OTC monograph not final part352 | Human OTC Drug Label | ||||||||
| 6 | Alba Sunblock Mineral Aloe Vanilla SPF 30 (Zinc Oxide, Titanium Dioxide) | The Hain Celestial Group, Inc. | Ver: 1 (R4) Jul 07, 2010 |
Cream | OTC monograph not final part352 | Human Prescription Drug Label | ||||||||
| 7 | Alba Sunblock Mineral FF SPF 30 (Zinc Oxide, Titanium Dioxide) | The Hain Celestial Group, Inc. | Ver: 1 (R4) Jul 03, 2010 |
Cream | OTC monograph not final part352 | Human OTC Drug Label | ||||||||
| 8 | Ambien (zolpidem tartrate) | Caremark L.L.C. | Ver: 1 (R4) Jan 27, 2010 |
Tablet, Film Coated | NDA NDA019908 | Human Prescription Drug Label | ||||||||
| 9 | Ambien (zolpidem tartrate) | Physicians Total Care, Inc. | Ver: 1 (R4) Jul 02, 2010 |
Tablet, Film Coated | NDA NDA019908 | Human Prescription Drug Label | ||||||||
| 10 | Ambien (zolpidem tartrate) | Rebel Distributors Corp. | Ver: 1 (R4) Jun 29, 2010 |
Tablet, Film Coated | NDA NDA019908 | Human Prescription Drug Label | ||||||||
| * indicates multiple versions of this label are available for viewing. Please click on label to see additional versions. | ||||||||||||||
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