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acetaminophen

NDC 68071-4172 · NuCare Pharmaceuticals,Inc.

Generic nameAcetaminophen
Dosage formSUPPOSITORY
RouteRECTAL
Active ingredient(s)ACETAMINOPHEN
Strength120 mg/1
Marketing categoryANDA

Packages

68071-4172-6 — 6 SUPPOSITORY in 1 BLISTER PACK (68071-4172-6)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 68071-3959 — ACETAMINOPHEN, 68071-4151 — 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, 68071-4941 — Hydrocodone Bitartrate and Acetaminophen, 68071-5010 — Acetaminophen and Codeine Phosphate, +3476 more

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