71335-1822 : Pregabalin 200 mg Oral Capsule

NDC:	71335-1822
Labeler:	Bryant Ranch Prepack
Product Type:	Human Prescription Drug
Drug Name:	Pregabalin
Dosage Form:	Oral Capsule
Application #:	ANDA206912
Rev. Date:	Oct 8, 2019
CSA Schedule:	CV (US) ^[1]

^[1] Schedule V Controlled Substance: Low potential for abuse relative to substances listed in Schedule IV and consist primarily of preparations containing limited quantities of certain narcotics. (i.e. Cough preparations containing not more than 200 milligrams of Codeine per 100 milliliters or per 100 grams [such as Robitussin AC, Phenergan with Codeine], and Ezogabine). More Details: US Dept of Justice Controlled Substance Schedules.

NDC Package Codes:

71335-1822-1: 30 CAPSULE IN 1 BOTTLE (71335‑1822‑1)
71335-1822-2: 60 CAPSULE IN 1 BOTTLE (71335‑1822‑2)
71335-1822-3: 90 CAPSULE IN 1 BOTTLE (71335‑1822‑3)

Active Ingredients:

Pregabalin

Dosage Strength:

200 mg

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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.

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