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AK-PENTOLATE
AK-PENTOLATE - 21695-883-15 - (Cyclopentolate Hydrochloride)
Drug Information of AK-PENTOLATE
| Product NDC: | 21695-883 |
| Proprietary Name: | AK-PENTOLATE |
| Non Proprietary Name: | Cyclopentolate Hydrochloride |
| Active Ingredient(s): | 10 mg/mL & nbsp; Cyclopentolate Hydrochloride |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | SOLUTION/ DROPS |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of AK-PENTOLATE
| Product NDC: | 21695-883 |
| Labeler Name: | Rebel Distributors Corp. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040164 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19970113 |
Package Information of AK-PENTOLATE
| Package NDC: | 21695-883-15 |
| Package Description: | 15 mL in 1 BOTTLE, DROPPER (21695-883-15) |
NDC Information of AK-PENTOLATE
| NDC Code | 21695-883-15 |
| Proprietary Name | AK-PENTOLATE |
| Package Description | 15 mL in 1 BOTTLE, DROPPER (21695-883-15) |
| Product NDC | 21695-883 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Cyclopentolate Hydrochloride |
| Dosage Form Name | SOLUTION/ DROPS |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 19970113 |
| Marketing Category Name | ANDA |
| Labeler Name | Rebel Distributors Corp. |
| Substance Name | CYCLOPENTOLATE HYDROCHLORIDE |
| Strength Number | 10 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
