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Pilocarpine Hydrochloride
Pilocarpine Hydrochloride - 64720-137-10 - (Pilocarpine Hydrochloride)
Drug Information of Pilocarpine Hydrochloride
| Product NDC: | 64720-137 |
| 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: | 64720-137 |
| Labeler Name: | CorePharma, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076746 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20041116 |
Package Information of Pilocarpine Hydrochloride
| Package NDC: | 64720-137-10 |
| Package Description: | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (64720-137-10) |
NDC Information of Pilocarpine Hydrochloride
| NDC Code | 64720-137-10 |
| Proprietary Name | Pilocarpine Hydrochloride |
| Package Description | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (64720-137-10) |
| Product NDC | 64720-137 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Pilocarpine Hydrochloride |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20041116 |
| Marketing Category Name | ANDA |
| Labeler Name | CorePharma, LLC |
| Substance Name | PILOCARPINE HYDROCHLORIDE |
| Strength Number | 5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Cholinergic Agonists [MoA],Cholinergic Muscarinic Agonists [MoA],Cholinergic Receptor Agonist [EPC] |
