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ACETAMINOPHEN

NDC 68071-3959 · NuCare Pharmaceuticals, Inc.

Generic nameACETAMINOPHEN
Dosage formTABLET
RouteORAL
Active ingredient(s)ACETAMINOPHEN
Strength500 mg/1
Marketing categoryOTC MONOGRAPH DRUG

Packages

68071-3959-1 — 1 BOTTLE in 1 CARTON (68071-3959-1) / 100 TABLET in 1 BOTTLE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

68071-3658 — acetaminophen and codeine phosphate, 68071-3683 — Oxycodone and Acetaminophen, 68071-3685 — Hydrocodone Bitartrate and Acetaminophen, 68071-3798 — Acetaminophen and Codeine Phosphate, 68071-3824 — Acetaminophen and Codeine Phosphate, 68071-3869 — Acetaminophen, 68071-3883 — Acetaminophen, 68071-3907 — Acetaminophen, 68071-3914 — Acetaminophen, Aspirin, Caffeine, 68071-3917 — 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, 68071-4801 — Hydrocodone Bitartrate and Acetaminophen, 68071-4853 — Hydrocodone Bitartrate and Acetaminophen, 68071-4860 — Acetaminophen, +3476 more

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