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J-MAX
J-MAX - 64661-011-16 - (Guaifenesin, and Phenylephrine Hydrochloride)
Drug Information of J-MAX
| Product NDC: | 64661-011 |
| Proprietary Name: | J-MAX |
| Non Proprietary Name: | Guaifenesin, and Phenylephrine Hydrochloride |
| Active Ingredient(s): | 200; 5 mg/5mL; mg/5mL & nbsp; Guaifenesin, and Phenylephrine Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SYRUP |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of J-MAX
| Product NDC: | 64661-011 |
| Labeler Name: | JayMac Pharmaceuticals LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20060314 |
Package Information of J-MAX
| Package NDC: | 64661-011-16 |
| Package Description: | 473 mL in 1 BOTTLE (64661-011-16) |
NDC Information of J-MAX
| NDC Code | 64661-011-16 |
| Proprietary Name | J-MAX |
| Package Description | 473 mL in 1 BOTTLE (64661-011-16) |
| Product NDC | 64661-011 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Guaifenesin, and Phenylephrine Hydrochloride |
| Dosage Form Name | SYRUP |
| Route Name | ORAL |
| Start Marketing Date | 20060314 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | JayMac Pharmaceuticals LLC |
| Substance Name | GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 200; 5 |
| Strength Unit | mg/5mL; mg/5mL |
| Pharmaceutical Classes |
