NDC 43386-118 – Hydrocodone Bitartrate and Homatropine Methylbromide

Hydrocodone Bitartrate 5 mg/1; Homatropine Methylbromide 1.5 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CII 1 recall

Product NDC43386-118

Product details

Brand name
Hydrocodone Bitartrate and Homatropine Methylbromide
Generic name
Hydrocodone Bitartrate and Homatropine Methylbromide
Labeler
Lupin Pharmaceuticals,Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA091528
Marketed since
September 23, 2014
Listing expires
December 31, 2026
Pharmacologic class
Opioid Agonist

Active ingredients

Uses, dosage, side effects and warnings for Hydrocodone Bitartrate and Homatropine Methylbromide →

Package NDC codes (2)

Package NDCDescriptionSince
43386-118-01 sample100 TABLET in 1 BOTTLE (43386-118-01)Sep 23, 2014
43386-118-03 sample30 TABLET in 1 BOTTLE (43386-118-03)Sep 23, 2014

Recalls mentioning this NDC

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