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NDC 43598-0071-01 Naproxen Sodium 220 mg/1 Details
Naproxen Sodium 220 mg/1
Naproxen Sodium is a ORAL TABLET, COATED in the HUMAN OTC DRUG category. It is labeled and distributed by Dr.Reddy's Laboratories Inc. The primary component is NAPROXEN SODIUM.
Product Information
NDC | 43598-0071 |
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Product ID | 43598-071_e944f1a0-dcbe-138e-6215-a35124ab36af |
Associated GPIs | |
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 | Naproxen Sodium |
Proprietary Name Suffix | Headache Pain |
Non-Proprietary Name | Naproxen Sodium |
Product Type | HUMAN OTC DRUG |
Dosage Form | TABLET, COATED |
Route | ORAL |
Active Ingredient Strength | 220 |
Active Ingredient Units | mg/1 |
Substance Name | NAPROXEN SODIUM |
Labeler Name | Dr.Reddy's Laboratories Inc |
Pharmaceutical Class | Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC] |
DEA Schedule | n/a |
Marketing Category | ANDA |
Application Number | ANDA075168 |
Listing Certified Through | 2024-12-31 |
Package
NDC 43598-0071-01 (43598007101)
NDC Package Code | 43598-071-01 |
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Billing NDC | 43598007101 |
Package | 1 BOTTLE in 1 CARTON (43598-071-01) / 100 TABLET, COATED in 1 BOTTLE |
Marketing Start Date | 2021-12-10 |
NDC Exclude Flag | N |
Pricing Information | N/A |