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Hydrocodone Bitartrate and Acetaminophen

NDC 68071-4801 · NuCare Pharmaceuticals,Inc.

Generic nameHydrocodone Bitartrate and Acetaminophen
Dosage formTABLET
RouteORAL
Active ingredient(s)HYDROCODONE BITARTRATE, ACETAMINOPHEN
Strength325; 5 mg/1; mg/1
Pharmacologic classOpioid Agonist [EPC], Opioid Agonists [MoA]
DEA scheduleCII
Marketing categoryANDA

Packages

68071-4801-2 — 12 TABLET in 1 BOTTLE (68071-4801-2)

68071-4801-6 — 6 TABLET in 1 BOTTLE (68071-4801-6)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

68071-3914 — Acetaminophen, Aspirin, Caffeine, 68071-3917 — Acetaminophen, 68071-3959 — ACETAMINOPHEN, 68071-4151 — Acetaminophen, 68071-4172 — Acetaminophen, 68071-4475 — acetaminophen and codeine phosphate, 68071-4533 — acetaminophen and codeine phosphate, 68071-4656 — Acetaminophen, 68071-4673 — Acetaminophen and Codeine Phosphate, 68071-4749 — Acetaminophen and Codeine Phosphate, 68071-4853 — Hydrocodone Bitartrate and Acetaminophen, 68071-4860 — Acetaminophen, 68071-4941 — Hydrocodone Bitartrate and Acetaminophen, 68071-5010 — Acetaminophen and Codeine Phosphate, 68071-5054 — Oxycodone and Acetaminophen, 68071-5169 — Oxycodone and Acetaminophen, 68071-5239 — Extra Strength Pain Relief, 68071-5300 — ACETAMINOPHEN, 68083-647 — Acetaminophen, 68083-648 — 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.