NDC 43386-356 – Hydrocodone Bitartrate and Acetaminophen

Hydrocodone Bitartrate 5 mg/1; Acetaminophen 325 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CII 1 recall

Product NDC43386-356

Product details

Brand name
Hydrocodone Bitartrate and Acetaminophen
Generic name
Hydrocodone Bitartrate and Acetaminophen
Labeler
Lupin Pharmaceuticals,Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA206245
Marketed since
December 1, 2016
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 (3)

Package NDCDescriptionSince
43386-356-01100 TABLET in 1 BOTTLE (43386-356-01)Dec 1, 2016
43386-356-05500 TABLET in 1 BOTTLE (43386-356-05)Dec 1, 2016
43386-356-101000 TABLET in 1 BOTTLE (43386-356-10)Dec 1, 2016

Recalls mentioning this NDC

Other Hydrocodone Bitartrate and Acetaminophen products