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AXID AR
AXID AR - 0573-2400-45 - (nizatidine)
Drug Information of AXID AR
| Product NDC: | 0573-2400 |
| Proprietary Name: | AXID AR |
| Non Proprietary Name: | nizatidine |
| Active Ingredient(s): | 75 mg/1 & nbsp; nizatidine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of AXID AR
| Product NDC: | 0573-2400 |
| Labeler Name: | Wyeth Consumer Healthcare |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | NDA020555 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19960509 |
Package Information of AXID AR
| Package NDC: | 0573-2400-45 |
| Package Description: | 1 BOTTLE, PLASTIC in 1 CARTON (0573-2400-45) > 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC |
NDC Information of AXID AR
| NDC Code | 0573-2400-45 |
| Proprietary Name | AXID AR |
| Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (0573-2400-45) > 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC |
| Product NDC | 0573-2400 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | nizatidine |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 19960509 |
| Marketing Category Name | NDA |
| Labeler Name | Wyeth Consumer Healthcare |
| Substance Name | NIZATIDINE |
| Strength Number | 75 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
