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AVAPTA
AVAPTA - 76332-004-03 - (HEXYLRESORCINOL)
Drug Information of AVAPTA
| Product NDC: | 76332-004 |
| Proprietary Name: | AVAPTA |
| Non Proprietary Name: | HEXYLRESORCINOL |
| Active Ingredient(s): | 1 mg/mL & nbsp; HEXYLRESORCINOL |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SPRAY |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of AVAPTA
| Product NDC: | 76332-004 |
| Labeler Name: | Neel Products LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part356 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20120816 |
Package Information of AVAPTA
| Package NDC: | 76332-004-03 |
| Package Description: | 59 mL in 1 BOTTLE (76332-004-03) |
NDC Information of AVAPTA
| NDC Code | 76332-004-03 |
| Proprietary Name | AVAPTA |
| Package Description | 59 mL in 1 BOTTLE (76332-004-03) |
| Product NDC | 76332-004 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | HEXYLRESORCINOL |
| Dosage Form Name | SPRAY |
| Route Name | ORAL |
| Start Marketing Date | 20120816 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Neel Products LLC |
| Substance Name | HEXYLRESORCINOL |
| Strength Number | 1 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
