0071-2418 : Zarontin 250 mg/5ml Oral Solution
| NDC: | 0071-2418 |
| Labeler: | Parke-davis Div of Pfizer Inc |
| Product Type: | Human Prescription Drug |
| Drug Name: |  Zarontin |
| Dosage Form: | Oral Solution |
| Application #: | ANDA080258 |
| Rev. Date: |
NDC Package Codes:
- 0071-2418-19: 1 BOTTLE, PLASTIC IN 1 CARTON (0071‑2418‑19) > 474 ML IN 1 BOTTLE, PLASTIC
- 0071-2418-23: 473 ML IN 1 BOTTLE (0071‑2418‑23)
- 0071-2418-35: 1 BOTTLE, PLASTIC IN 1 CARTON (0071‑2418‑35) > 474 ML IN 1 BOTTLE, PLASTIC
Active Ingredients:
- Ethosuximide
Dosage Strength:
- 250 mg/5mL
Pharmaceutical Classes:
- Anti-epileptic Agent [EPC]
- Decreased Central Nervous System Disorganized Electrical Activity [PE]
Related Products:
Based on records with the same trade name.- 0071-0237 Zarontin 250 mg Oral Capsule by Parke-davis Div of Pfizer Inc
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Ethosuximide
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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.