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Pediaderm HC
Pediaderm HC - 24338-420-01 - (Hydrocortisone)
Drug Information of Pediaderm HC
| Product NDC: | 24338-420 |
| Proprietary Name: | Pediaderm HC |
| Non Proprietary Name: | Hydrocortisone |
| Active Ingredient(s): | & nbsp; Hydrocortisone |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Pediaderm HC
| Product NDC: | 24338-420 |
| Labeler Name: | Arbor Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA083231 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20091102 |
Package Information of Pediaderm HC
| Package NDC: | 24338-420-01 |
| Package Description: | 1 KIT in 1 CARTON (24338-420-01) * 29.6 mL in 1 TUBE (24338-316-30) * 85 g in 1 TUBE |
NDC Information of Pediaderm HC
| NDC Code | 24338-420-01 |
| Proprietary Name | Pediaderm HC |
| Package Description | 1 KIT in 1 CARTON (24338-420-01) * 29.6 mL in 1 TUBE (24338-316-30) * 85 g in 1 TUBE |
| Product NDC | 24338-420 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Hydrocortisone |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20091102 |
| Marketing Category Name | ANDA |
| Labeler Name | Arbor Pharmaceuticals, Inc. |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
