NDC 31722-997 – Hydrocodone Bitartrate and Acetaminophen

Hydrocodone Bitartrate 10 mg/1; Acetaminophen 325 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CII 1 recall

Product NDC31722-997

Product details

Brand name
Hydrocodone Bitartrate and Acetaminophen
Generic name
Hydrocodone Bitartrate and Acetaminophen
Labeler
Camber Pharmaceuticals, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA211487
Marketed since
November 8, 2018
Listing expires
December 31, 2026
Pharmacologic class
Opioid Agonist

Active ingredients

Uses, dosage, side effects and warnings for Hydrocodone Bitartrate and Acetaminophen →

Package NDC codes (2)

Package NDCDescriptionSince
31722-997-01100 TABLET in 1 BOTTLE (31722-997-01)Nov 8, 2018
31722-997-05500 TABLET in 1 BOTTLE (31722-997-05)Nov 8, 2018

Recalls mentioning this NDC

Other Hydrocodone Bitartrate and Acetaminophen products