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Cyclomydril
Cyclomydril - 0065-0359-02 - (cyclopentolate hydrochloride and phenylephrine hydrochloride)
Drug Information of Cyclomydril
| Product NDC: | 0065-0359 |
| Proprietary Name: | Cyclomydril |
| Non Proprietary Name: | cyclopentolate hydrochloride and phenylephrine hydrochloride |
| Active Ingredient(s): | 2; 10 mg/mL; mg/mL & nbsp; cyclopentolate hydrochloride and phenylephrine hydrochloride |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | SOLUTION/ DROPS |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Cyclomydril
| Product NDC: | 0065-0359 |
| Labeler Name: | Alcon Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA084300 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19580630 |
Package Information of Cyclomydril
| Package NDC: | 0065-0359-02 |
| Package Description: | 2 mL in 1 BOTTLE, PLASTIC (0065-0359-02) |
NDC Information of Cyclomydril
| NDC Code | 0065-0359-02 |
| Proprietary Name | Cyclomydril |
| Package Description | 2 mL in 1 BOTTLE, PLASTIC (0065-0359-02) |
| Product NDC | 0065-0359 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | cyclopentolate hydrochloride and phenylephrine hydrochloride |
| Dosage Form Name | SOLUTION/ DROPS |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 19580630 |
| Marketing Category Name | ANDA |
| Labeler Name | Alcon Laboratories, Inc. |
| Substance Name | CYCLOPENTOLATE HYDROCHLORIDE; PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 2; 10 |
| Strength Unit | mg/mL; mg/mL |
| Pharmaceutical Classes |
