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Hydrocodone Bitartrate and Acetaminophen

NDC 68071-2494 · NuCare Pharmaceuticals,Inc.

Generic nameHydrocodone Bitartrate and Acetaminophen
Dosage formTABLET
RouteORAL
Active ingredient(s)HYDROCODONE BITARTRATE, ACETAMINOPHEN
Strength325; 7.5 mg/1; mg/1
Pharmacologic classOpioid Agonist [EPC], Opioid Agonists [MoA]
DEA scheduleCII
Marketing categoryANDA

Packages

68071-2494-2 — 12 TABLET in 1 BOTTLE (68071-2494-2)

68071-2494-6 — 6 TABLET in 1 BOTTLE (68071-2494-6)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

68016-303 — Acetaminophen, 68016-543 — Acetaminophen, 68016-654 — Acetaminophen Diphenhydramine HCl, 68016-734 — Acetaminophen, 68016-797 — Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl, 68016-877 — Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride, 68016-878 — Acetaminophen, Dextromethorphan HBr and Doxylamine Succinate, 68047-721 — butalbital and acetaminophen, 68047-752 — butalbital and acetaminophen, 68047-753 — butalbital and acetaminophen, 68071-2645 — Hydrocodone Bitartrate and Acetaminophen, 68071-3249 — Butalbital, Acetaminophen, and Caffeine, 68071-3437 — Acetaminophen, 68071-3447 — Hydrocodone Bitartrate and Acetaminophen, 68071-3454 — Acetaminophen, 68071-3565 — Acetaminophen, 68071-3651 — acetaminophen and codeine phosphate, 68071-3658 — acetaminophen and codeine phosphate, 68071-3683 — Oxycodone and Acetaminophen, 68071-3685 — Hydrocodone Bitartrate and Acetaminophen, +3514 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.