NDC 10702-055 – 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 NDC10702-055

Product details

Brand name
Hydrocodone Bitartrate and Homatropine Methylbromide
Generic name
Hydrocodone Bitartrate and Homatropine Methylbromide
Labeler
KVK-Tech, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA207176
Marketed since
August 7, 2017
Listing expires
December 31, 2027
Pharmacologic class
Opioid Agonist

Active ingredients

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

Package NDC codes (4)

Package NDCDescriptionSince
10702-055-01100 TABLET in 1 BOTTLE (10702-055-01)Aug 7, 2017
10702-055-0330 TABLET in 1 BOTTLE (10702-055-03)Aug 7, 2017
10702-055-0990 TABLET in 1 BOTTLE (10702-055-09)Aug 7, 2017
10702-055-101000 TABLET in 1 BOTTLE (10702-055-10)Aug 7, 2017

Recalls mentioning this NDC

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