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Effervescent Pain Relief
Effervescent Pain Relief - 62982-002-12 - (Aspirin, Citric Acid Monohydrate, and Sodium Bicarbonate)
Drug Information of Effervescent Pain Relief
| Product NDC: | 62982-002 |
| Proprietary Name: | Effervescent Pain Relief |
| Non Proprietary Name: | Aspirin, Citric Acid Monohydrate, and Sodium Bicarbonate |
| Active Ingredient(s): | 325; 1000; 1916 mg/1; mg/1; mg/1 & nbsp; Aspirin, Citric Acid Monohydrate, and Sodium Bicarbonate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, EFFERVESCENT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Effervescent Pain Relief
| Product NDC: | 62982-002 |
| Labeler Name: | Deseret Laboratories, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part343 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20060922 |
Package Information of Effervescent Pain Relief
| Package NDC: | 62982-002-12 |
| Package Description: | 12 PACKET in 1 BOX (62982-002-12) > 2 TABLET, EFFERVESCENT in 1 PACKET |
NDC Information of Effervescent Pain Relief
| NDC Code | 62982-002-12 |
| Proprietary Name | Effervescent Pain Relief |
| Package Description | 12 PACKET in 1 BOX (62982-002-12) > 2 TABLET, EFFERVESCENT in 1 PACKET |
| Product NDC | 62982-002 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Aspirin, Citric Acid Monohydrate, and Sodium Bicarbonate |
| Dosage Form Name | TABLET, EFFERVESCENT |
| Route Name | ORAL |
| Start Marketing Date | 20060922 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Deseret Laboratories, Inc. |
| Substance Name | ASPIRIN; CITRIC ACID MONOHYDRATE; SODIUM BICARBONATE |
| Strength Number | 325; 1000; 1916 |
| Strength Unit | mg/1; mg/1; mg/1 |
| Pharmaceutical Classes |
