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Dicyclomine Hydrochloride
Dicyclomine Hydrochloride - 52125-517-03 - (Dicyclomine Hydrochloride)
Drug Information of Dicyclomine Hydrochloride
| Product NDC: | 52125-517 |
| Proprietary Name: | Dicyclomine Hydrochloride |
| Non Proprietary Name: | Dicyclomine Hydrochloride |
| Active Ingredient(s): | 20 mg/1 & nbsp; Dicyclomine Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Dicyclomine Hydrochloride
| Product NDC: | 52125-517 |
| Labeler Name: | REMEDYREPACK INC. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA085223 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130624 |
Package Information of Dicyclomine Hydrochloride
| Package NDC: | 52125-517-03 |
| Package Description: | 20 TABLET in 1 VIAL (52125-517-03) |
NDC Information of Dicyclomine Hydrochloride
| NDC Code | 52125-517-03 |
| Proprietary Name | Dicyclomine Hydrochloride |
| Package Description | 20 TABLET in 1 VIAL (52125-517-03) |
| Product NDC | 52125-517 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Dicyclomine Hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20130624 |
| Marketing Category Name | ANDA |
| Labeler Name | REMEDYREPACK INC. |
| Substance Name | DICYCLOMINE HYDROCHLORIDE |
| Strength Number | 20 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Anticholinergic [EPC],Cholinergic Antagonists [MoA] |
