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Hydrocortisone and Acetic Acid
Hydrocortisone and Acetic Acid - 0603-7039-39 - (hydrocortisone and acetic acid)
Drug Information of Hydrocortisone and Acetic Acid
| Product NDC: | 0603-7039 |
| Proprietary Name: | Hydrocortisone and Acetic Acid |
| Non Proprietary Name: | hydrocortisone and acetic acid |
| Active Ingredient(s): | .02; .01 mL/mL; mL/mL & nbsp; hydrocortisone and acetic acid |
| Administration Route(s): | AURICULAR (OTIC) |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Hydrocortisone and Acetic Acid
| Product NDC: | 0603-7039 |
| Labeler Name: | Qualitest Pharmaceuticals |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040609 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20060206 |
Package Information of Hydrocortisone and Acetic Acid
| Package NDC: | 0603-7039-39 |
| Package Description: | 10 mL in 1 BOTTLE, DROPPER (0603-7039-39) |
NDC Information of Hydrocortisone and Acetic Acid
| NDC Code | 0603-7039-39 |
| Proprietary Name | Hydrocortisone and Acetic Acid |
| Package Description | 10 mL in 1 BOTTLE, DROPPER (0603-7039-39) |
| Product NDC | 0603-7039 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | hydrocortisone and acetic acid |
| Dosage Form Name | SOLUTION |
| Route Name | AURICULAR (OTIC) |
| Start Marketing Date | 20060206 |
| Marketing Category Name | ANDA |
| Labeler Name | Qualitest Pharmaceuticals |
| Substance Name | ACETIC ACID; HYDROCORTISONE |
| Strength Number | .02; .01 |
| Strength Unit | mL/mL; mL/mL |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
