Hydrocodone Bitartrate and Acetaminophen NDC 13107-211

NDC codes

FDA NDC Directory

Product NDC (as listed)13107-211Labeler and product segments. Claims need a package NDC.

Product NDC at billing width13107-0211Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package
13107-211-01	13107021101	100 TABLET in 1 BOTTLE (13107-211-01)Marketed from May 6, 2015
13107-211-05	13107021105	500 TABLET in 1 BOTTLE (13107-211-05)Marketed from May 6, 2015
13107-211-30	13107021130	30 TABLET in 1 BOTTLE (13107-211-30)Marketed from May 6, 2015
13107-211-99	13107021199	1000 TABLET in 1 BOTTLE (13107-211-99)Marketed from May 6, 2015

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary): Hydrocodone Bitartrate and Acetaminophen
Generic name (nonproprietary): hydrocodone bitartrate and acetaminophen
Active ingredients: Hydrocodone bitartrate — 5 mg/1Acetaminophen — 300 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Aurolife Pharma, LLC
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 207709
Marketing start: May 6, 2015
Listing expires: Dec 31, 2026
DEA schedule: CII
Other FDA classes: Opioid Agonists (Mechanism)
Identifiers: Product ID 13107-211_265ff2e7-c060-4a82-909b-26e71c262dd6SPL ID 265ff2e7-c060-4a82-909b-26e71c262dd6SPL set ID 392a846e-7325-462d-b19b-8afda44c5cb0RxCUI 856980, 856987, 856992UNII NO70W886KK, 362O9ITL9DUPC 0313107213014, 0313107211010
Pharmacologic class: Opioid Agonist

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N413107021101 followed by a unit qualifier and the quantity

Package 13107-0211-01. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective Dec 17, 2025. This label includes a boxed warning.

Indications (excerpt from the label)

INDICATIONS AND USAGE Hydrocodone bitartrate and acetaminophen tablets are indicated for the management of pain severe enough to require an opioid analgesic and for which alternative treatments are inadequate. Limitations of Use Because of the risks of addiction, abuse, and misuse, overdose and death, which can occur at any dosage or duration and persist over the course of therapy [see WARNINGS ], reserve opioid analgesics, including hydrocodone bitartrate and acetaminophen tablets for use in patients for whom alternative treatment options are ineffective, not tolerated, or would be otherwise inadequate to provide sufficient management of pain. .

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 207709

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

FDA NDC Directory listings under ANDA 207709
Product	Strength	Form · route	Labeler	Product NDC
Hydrocodone Bitartrate and Acetaminophen	Hydrocodone bitartrate 7.5 mg/1; Acetaminophen 300 mg/1	TabletOral	Aurolife Pharma, LLC	13107-212
Hydrocodone Bitartrate and Acetaminophen	Hydrocodone bitartrate 10 mg/1; Acetaminophen 300 mg/1	TabletOral	Aurolife Pharma, LLC	13107-213