Class II · Moderate risk
Rising
Presence of Precipitate: medication was crystallizing and particles floating in the bottle
National Drug Code
Is NDC 64980-0504-48 recalled?
Cyproheptadine Hydrochloride · 473 mL in 1 BOTTLE (64980-504-48)
Yes — this exact package was recalled
2 FDA recalls name the code 64980-0504-48 directly. A recall still applies to particular lot numbers — compare the lot on your package with the FDA notice below, and talk to your pharmacist before stopping a prescribed medication.
1 of these recalls is still ongoing.
- Active ingredient
- Cyproheptadine Hydrochloride
- Strength
- CYPROHEPTADINE HYDROCHLORIDE 2 mg/5mL
- Form
- Syrup · Oral
- Labeler
- Rising Pharma Holdings, Inc.
- Type
- Human Prescription Drug
- Product code
- 64980-0504
Recalls naming this package
Class III · Low risk
Cyproheptadine Hydrochloride Syrup
Subpotency: product assayed and found OOS for cyproheptadine
Where to find this code. The NDC is printed on the pharmacy label and on the manufacturer's carton, usually as three groups of digits after “NDC”. The last group is the package size — two bottles of the same medicine can differ only in that group, and a recall may cover one but not the other.
Other recalled products from this labeler
- 64980-0514 Timolol Maleate 8
- 64980-0513 Timolol Maleate 2
- 64980-0599 Chlorthalidone 2
- 64980-0104 Dibasic Sodium Phosphate, Monobasic Potassium Phosphate and Monobasic Sodium Phosphate 1
- 64980-0124 Diflorasone Diacetate 1
- 64980-0129 See recall 1
Free recall alerts
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