FDA Orange Book
Generic for Moviprep
Moviprep contains ascorbic acid, polyethylene glycol 3350, potassium chloride, sodium ascorbate, sodium chloride and sodium sulfate. Orange Book status for every listed strength, the approved generic makers, and the listed patents and exclusivities.
Source: FDA Orange Book data file dated 2026-10-09. Publisher page
Yes. The generic name for Moviprep is ascorbic acid, polyethylene glycol 3350, potassium chloride, sodium ascorbate, sodium chloride and sodium sulfate. 1 company holds an active FDA approval (ANDA) for a generic version in the Orange Book. Therapeutic equivalence codes: AA.
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Moviprep products in the Orange Book
| Form and route | Strength | Brand status | Brand TE | Active generics | Generic TE codes |
|---|---|---|---|---|---|
| for solution, oral | 4.7GM;100GM;1.015GM;5.9GM;2.691GM;7.5GM | Marketed (Rx) | AA | 1 | AA |
NDA 021881, held by SALIX PHARMACEUTICALS INC. Active generics are ANDA products in the Orange Book prescription list with the same ingredient, dosage form, route and strength.
Approved generic ascorbic acid, polyethylene glycol 3350, potassium chloride, sodium ascorbate, sodium chloride and sodium sulfate
| Company | ANDA | TE code | Approved | Strengths |
|---|---|---|---|---|
| NOVEL LABORATORIES INC | 090145 | AA (A-rated, therapeutically equivalent) | January 25, 2012 | 4.7GM;100GM;1.015GM;5.9GM;2.691GM;7.5GM |
Questions
Is there a generic for Moviprep?
Yes. The generic name for Moviprep is ascorbic acid, polyethylene glycol 3350, potassium chloride, sodium ascorbate, sodium chloride and sodium sulfate. 1 company holds an active FDA approval (ANDA) for a generic version in the Orange Book. Therapeutic equivalence codes: AA.
What is the generic name for Moviprep?
The active ingredient in Moviprep is ascorbic acid, polyethylene glycol 3350, potassium chloride, sodium ascorbate, sodium chloride and sodium sulfate, per the FDA Orange Book.
What does a therapeutic equivalence code mean?
In the Orange Book, codes that start with A (such as AB) mean FDA considers the product therapeutically equivalent to the reference drug. Codes that start with B mean FDA does not, at this time, consider the product therapeutically equivalent.