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NDC 50201-0421-02 Bromo Seltzer 1000; 325; 1916 mg/1; mg/1; mg/1 Details
Bromo Seltzer 1000; 325; 1916 mg/1; mg/1; mg/1
Bromo Seltzer is a ORAL TABLET, EFFERVESCENT in the HUMAN OTC DRUG category. It is labeled and distributed by Tower Laboratories Ltd. The primary component is ANHYDROUS CITRIC ACID; ASPIRIN; SODIUM BICARBONATE.
Product Information
NDC | 50201-0421 |
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Product ID | 50201-0421_f0306b64-e6f7-476c-e053-2a95a90a2576 |
Associated GPIs | 64109902110820 |
GCN Sequence Number | n/a |
GCN Sequence Number Description | n/a |
HIC3 | n/a |
HIC3 Description | n/a |
GCN | n/a |
HICL Sequence Number | n/a |
HICL Sequence Number Description | n/a |
Brand/Generic | n/a |
Proprietary Name | Bromo Seltzer |
Proprietary Name Suffix | n/a |
Non-Proprietary Name | ASPIRIN, SODIUM BICARBONATE, CITRIC ACID |
Product Type | HUMAN OTC DRUG |
Dosage Form | TABLET, EFFERVESCENT |
Route | ORAL |
Active Ingredient Strength | 1000; 325; 1916 |
Active Ingredient Units | mg/1; mg/1; mg/1 |
Substance Name | ANHYDROUS CITRIC ACID; ASPIRIN; SODIUM BICARBONATE |
Labeler Name | Tower Laboratories Ltd |
Pharmaceutical Class | Acidifying Activity [MoA], Alkalinizing Activity [MoA], Anti-Inflammatory Agents, Non-Steroidal [CS], Anti-coagulant [EPC], Calcium Chelating Activity [MoA], Calculi Dissolution Agent [EPC], Cyclooxygenase Inhibitors [MoA], Decreased Coagulation Factor Ac |
DEA Schedule | n/a |
Marketing Category | OTC MONOGRAPH FINAL |
Application Number | part343 |
Listing Certified Through | 2024-12-31 |
Package
NDC 50201-0421-02 (50201042102)
NDC Package Code | 50201-0421-2 |
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Billing NDC | 50201042102 |
Package | 10 POUCH in 1 CARTON (50201-0421-2) / 2 TABLET, EFFERVESCENT in 1 POUCH |
Marketing Start Date | 2012-07-16 |
NDC Exclude Flag | N |
Pricing Information | N/A |