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albuterol sulfate
albuterol sulfate - 52125-235-08 - (albuterol sulfate)
Drug Information of albuterol sulfate
| Product NDC: | 52125-235 |
| Proprietary Name: | albuterol sulfate |
| Non Proprietary Name: | albuterol sulfate |
| Active Ingredient(s): | 2 mg/1 & nbsp; albuterol sulfate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of albuterol sulfate
| Product NDC: | 52125-235 |
| Labeler Name: | REMEDYREPACK INC. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA072637 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130306 |
Package Information of albuterol sulfate
| Package NDC: | 52125-235-08 |
| Package Description: | 10 TABLET in 1 BLISTER PACK (52125-235-08) |
NDC Information of albuterol sulfate
| NDC Code | 52125-235-08 |
| Proprietary Name | albuterol sulfate |
| Package Description | 10 TABLET in 1 BLISTER PACK (52125-235-08) |
| Product NDC | 52125-235 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | albuterol sulfate |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20130306 |
| Marketing Category Name | ANDA |
| Labeler Name | REMEDYREPACK INC. |
| Substance Name | ALBUTEROL SULFATE |
| Strength Number | 2 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Adrenergic beta2-Agonists [MoA],beta2-Adrenergic Agonist [EPC] |
