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Pilocarpine Hydrochloride
Pilocarpine Hydrochloride - 0115-5922-03 - (PILOCARPINE HYDROCHLORIDE)
Drug Information of Pilocarpine Hydrochloride
| Product NDC: | 0115-5922 |
| Proprietary Name: | Pilocarpine Hydrochloride |
| Non Proprietary Name: | PILOCARPINE HYDROCHLORIDE |
| Active Ingredient(s): | 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: | 0115-5922 |
| Labeler Name: | Global Pharmaceuticals, Division of Impax Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077248 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20070501 |
Package Information of Pilocarpine Hydrochloride
| Package NDC: | 0115-5922-03 |
| Package Description: | 1000 TABLET, FILM COATED in 1 BOTTLE (0115-5922-03) |
NDC Information of Pilocarpine Hydrochloride
| NDC Code | 0115-5922-03 |
| Proprietary Name | Pilocarpine Hydrochloride |
| Package Description | 1000 TABLET, FILM COATED in 1 BOTTLE (0115-5922-03) |
| Product NDC | 0115-5922 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | PILOCARPINE HYDROCHLORIDE |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20070501 |
| Marketing Category Name | ANDA |
| Labeler Name | Global Pharmaceuticals, Division of Impax Laboratories, Inc. |
| Substance Name | PILOCARPINE HYDROCHLORIDE |
| Strength Number | 5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Cholinergic Agonists [MoA],Cholinergic Muscarinic Agonists [MoA],Cholinergic Receptor Agonist [EPC] |
