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Pilocarpine hydrochloride
Pilocarpine hydrochloride - 0228-2837-11 - (Pilocarpine hydrochloride)
Drug Information of Pilocarpine hydrochloride
| Product NDC: | 0228-2837 |
| Proprietary Name: | Pilocarpine hydrochloride |
| Non Proprietary Name: | Pilocarpine hydrochloride |
| Active Ingredient(s): | 7.5 mg/1 & nbsp; Pilocarpine hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Pilocarpine hydrochloride
| Product NDC: | 0228-2837 |
| Labeler Name: | Actavis Elizabeth LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020237 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20110913 |
Package Information of Pilocarpine hydrochloride
| Package NDC: | 0228-2837-11 |
| Package Description: | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0228-2837-11) |
NDC Information of Pilocarpine hydrochloride
| NDC Code | 0228-2837-11 |
| Proprietary Name | Pilocarpine hydrochloride |
| Package Description | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0228-2837-11) |
| Product NDC | 0228-2837 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Pilocarpine hydrochloride |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20110913 |
| Marketing Category Name | NDA |
| Labeler Name | Actavis Elizabeth LLC |
| Substance Name | PILOCARPINE HYDROCHLORIDE |
| Strength Number | 7.5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Cholinergic Agonists [MoA],Cholinergic Muscarinic Agonists [MoA],Cholinergic Receptor Agonist [EPC] |
