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Alka-Seltzer XTRA STRENGTH
Alka-Seltzer XTRA STRENGTH - 0280-4035-12 - (Anhydrous Citric Acid, Sodium Bicarbonate, and Aspirin)
Drug Information of Alka-Seltzer XTRA STRENGTH
| Product NDC: | 0280-4035 |
| Proprietary Name: | Alka-Seltzer XTRA STRENGTH |
| Non Proprietary Name: | Anhydrous Citric Acid, Sodium Bicarbonate, and Aspirin |
| Active Ingredient(s): | 1000; 500; 1985 mg/1; mg/1; mg/1 & nbsp; Anhydrous Citric Acid, Sodium Bicarbonate, and Aspirin |
| Administration Route(s): | ORAL |
| Dosage Form(s): | GRANULE, EFFERVESCENT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Alka-Seltzer XTRA STRENGTH
| Product NDC: | 0280-4035 |
| Labeler Name: | Bayer HealthCare LLC, Consumer Care |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100302 |
Package Information of Alka-Seltzer XTRA STRENGTH
| Package NDC: | 0280-4035-12 |
| Package Description: | 12 PACKET in 1 CARTON (0280-4035-12) > 1 GRANULE, EFFERVESCENT in 1 PACKET |
NDC Information of Alka-Seltzer XTRA STRENGTH
| NDC Code | 0280-4035-12 |
| Proprietary Name | Alka-Seltzer XTRA STRENGTH |
| Package Description | 12 PACKET in 1 CARTON (0280-4035-12) > 1 GRANULE, EFFERVESCENT in 1 PACKET |
| Product NDC | 0280-4035 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Anhydrous Citric Acid, Sodium Bicarbonate, and Aspirin |
| Dosage Form Name | GRANULE, EFFERVESCENT |
| Route Name | ORAL |
| Start Marketing Date | 20100302 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Bayer HealthCare LLC, Consumer Care |
| Substance Name | ANHYDROUS CITRIC ACID; ASPIRIN; SODIUM BICARBONATE |
| Strength Number | 1000; 500; 1985 |
| Strength Unit | mg/1; mg/1; mg/1 |
| Pharmaceutical Classes |
