NDC codes

FDA NDC Directory
Product NDC (as listed)70710-1048Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70710-1048Add 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 NDC11-digit (billing)PackageCopy
70710-1048-170710104801100 TABLET, FILM COATED in 1 BOTTLE (70710-1048-1)Marketed from Jun 30, 2023
70710-1048-37071010480330 TABLET, FILM COATED in 1 BOTTLE (70710-1048-3)Marketed from Jun 30, 2023
70710-1048-570710104805500 TABLET, FILM COATED in 1 BOTTLE (70710-1048-5)Marketed from Jun 30, 2023

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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)
Erythromycin
Generic name (nonproprietary)
erythromycin
Active ingredients
Erythromycin — 500 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Labeler
Zydus Pharmaceuticals USA Inc.NDC labeler code 70710
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 212693
Marketing start
Listing expires
Other FDA classes
Decreased Sebaceous Gland Activity (Physiologic effect)Macrolides (Chemical structure)
Identifiers
Product ID 70710-1048_98d365a7-fc2c-4602-aef6-a604c82252c7SPL ID 98d365a7-fc2c-4602-aef6-a604c82252c7SPL set ID 0277341c-8513-4317-9334-c242f97630c1RxCUI 197650, 598006UNII 63937KV33D
Pharmacologic class
Macrolide Antimicrobial; Macrolide

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

N470710104801 followed by a unit qualifier and the quantity

Package 70710-1048-01. 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 .

Indications (excerpt from the label)

INDICATIONS AND USAGE To reduce the development of drug-resistant bacteria and maintain the effectiveness of erythromycin tablets, USP and other antibacterial drugs, erythromycin tablets, USP should be used only to treat or prevent infections that are proven or strongly suspected to be caused by susceptible bacteria. When culture and susceptibility information are available, they should be considered in selecting or modifying antibacterial therapy. In the absence of such data, local epidemiology and susceptibility patterns may contribute to the empiric selection of therapy. Erythromycin tablets, USP are indicated in the treatment of infections caused by susceptible strains of the designated …

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 70710-1048

What is NDC 70710-1048?
70710-1048 is the product NDC for Erythromycin, Erythromycin 500 mg/1 tablet, film coated, listed with the FDA by Zydus Pharmaceuticals USA Inc.. It has 3 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Erythromycin.
What is the active ingredient?
Erythromycin.
Who is the labeler?
Zydus Pharmaceuticals USA Inc., NDC labeler code 70710. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Erythromycin?
68 other product NDCs are listed under this name. See all Erythromycin NDCs.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Erythromycin NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
ErythromycinErythromycin 5 mg/gOintmentOphthalmicSentiss Pharmaceuticals LLC70244-03170244-0031-0170244-0031-02
ErythromycinErythromycin 333 mg/1Tablet, Delayed releaseOralTorrent Pharmaceuticals Limited13668-58713668-0587-0113668-0587-0513668-0587-30
erythromycinErythromycin 250 mg/1Capsule, Delayed release pelletsOralDr. Reddy's Labratories Inc.75907-07675907-0076-01
ErythromycinErythromycin 5 mg/gOintmentOphthalmicST. MARY'S MEDICAL PARK PHARMACY60760-67060760-0670-35
ErythromycinErythromycin 5 mg/gOintmentOphthalmicRedpharm Drug67296-212867296-2128-03
ErythromycinErythromycin 5 mg/gOintmentOphthalmicNuCare Pharmaceuticals,Inc.68071-399268071-3992-02
ErythromycinErythromycin 5 mg/gOintmentOphthalmicARMAS PHARMACEUTICALS INC.72485-67072485-0670-3172485-0670-35
ErythromycinErythromycin 5 mg/gOintmentOphthalmicFera Pharmaceuticals, LLC48102-05748102-0057-11
ErythromycinErythromycin 250 mg/1Tablet, Film coatedOralAlembic Pharmaceuticals Limited46708-39746708-0397-3046708-0397-3146708-0397-91
ErythromycinErythromycin 500 mg/1Tablet, Film coatedOralAlembic Pharmaceuticals Limited46708-39846708-0398-3046708-0398-3146708-0398-91

All 69 Erythromycin NDCs

Other NDCs under ANDA 212693

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

FDA NDC Directory listings under ANDA 212693
ProductStrengthForm · routeLabelerProduct NDC
ErythromycinErythromycin 250 mg/1Tablet, Film coatedOralZydus Pharmaceuticals USA Inc.70710-1047
ErythromycinErythromycin 250 mg/1Tablet, Film coatedOralZydus Lifesciences Limited70771-1548
ErythromycinErythromycin 500 mg/1Tablet, Film coatedOralZydus Lifesciences Limited70771-1549

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