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Baczol Expectorant
Baczol Expectorant - 49523-501-04 - (GUAIFENESIN and PHENYLEPHRINE HYDROCHLORIDE)
Drug Information of Baczol Expectorant
| Product NDC: | 49523-501 |
| Proprietary Name: | Baczol Expectorant |
| 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): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Baczol Expectorant
| Product NDC: | 49523-501 |
| Labeler Name: | Lex Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20130204 |
Package Information of Baczol Expectorant
| Package NDC: | 49523-501-04 |
| Package Description: | 1 BOTTLE in 1 CARTON (49523-501-04) > 120 mL in 1 BOTTLE |
NDC Information of Baczol Expectorant
| NDC Code | 49523-501-04 |
| Proprietary Name | Baczol Expectorant |
| Package Description | 1 BOTTLE in 1 CARTON (49523-501-04) > 120 mL in 1 BOTTLE |
| Product NDC | 49523-501 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | GUAIFENESIN and PHENYLEPHRINE HYDROCHLORIDE |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20130204 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Lex Inc |
| Substance Name | GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 200; 5 |
| Strength Unit | mg/5mL; mg/5mL |
| Pharmaceutical Classes |
