Over-the-counter drug · OTC MONOGRAPH DRUG
Extra Strength Pain Relief (Acetaminophen) NDC 68788-8375
Acetaminophen 500 mg/15mL · Suspension · Oral · Preferred Pharmaceuticals Inc.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 68788-8375-2 | 6878883750268788837502 | 237 mL in 1 BOTTLE (68788-8375-2)Marketed from Feb 24, 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)
- Extra Strength Pain Relief
- Generic name (nonproprietary)
- acetaminophen
- Active ingredients
- Acetaminophen — 500 mg/15mL
- Dosage form
- Suspension
- Route
- Oral
- Labeler
- Preferred Pharmaceuticals Inc.NDC labeler code 68788
- Product type
- Over-the-counter drug
- Marketing category
- OTC monograph drugApplication 343
- Marketing start
- Listing expires
- Identifiers
- Product ID 68788-8375_87ba6c74-963f-4b18-b22e-5577a701daf7SPL ID 87ba6c74-963f-4b18-b22e-5577a701daf7SPL set ID e18294f5-8fd5-4ac6-802c-f6d257e8bee7UNII 362O9ITL9D
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
N468788837502followed by a unit qualifier and the quantityPackage 68788-8375-02. 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)
Uses • temporarily relieves minor aches and pains • temporarily reduces fever
Excerpt only. Read the full label for complete information.
About NDC 68788-8375
- What is NDC 68788-8375?
- 68788-8375 is the product NDC for Extra Strength Pain Relief (acetaminophen), Acetaminophen 500 mg/15mL suspension, listed with the FDA by Preferred Pharmaceuticals Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Extra Strength Pain Relief (Acetaminophen).
- What is the active ingredient?
- Acetaminophen.
- Who is the labeler?
- Preferred Pharmaceuticals Inc., NDC labeler code 68788. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Extra Strength Pain Relief?
- 10 other product NDCs are listed under this name. See all Extra Strength Pain Relief NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other Extra Strength Pain Relief products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| Extra Strength Pain Reliefacetaminophen | Acetaminophen 500 mg/1 | TabletOral | Preferred Pharmaceuticals Inc. | 68788-8786 | 68788-8786-0168788-8786-0268788-8786-03+1 more |
| Extra Strength Pain Reliefacetaminophen, aspirin, caffeine | Aspirin 250 mg/1 + 2 more ingredients | TabletOral | BETTER LIVING BRANDS, LLC | 21130-037 | 21130-0037-0121130-0037-2021130-0037-42 |
| Extra Strength Pain Reliefacetaminophen | Acetaminophen 500 mg/15mL | SuspensionOral | GERI-CARE PHARMACEUTICAL CORP | 57896-206 | 57896-0206-08 |
| Extra Strength Pain Reliefacetaminophen | Acetaminophen 500 mg/1 | Tablet, CoatedOral | VALU MERCHANDISERS COMPANY | 63941-104 | 63941-0104-0163941-0104-0263941-0104-04+2 more |
| Extra Strength Pain Reliefacetaminophen | Acetaminophen 500 mg/1 | TabletOral | VALU MERCHANDISERS COMPANY | 63941-303 | 63941-0303-04 |
| Extra Strength Pain Reliefacetaminophen | Acetaminophen 500 mg/1 | Tablet, CoatedOral | VALU MERCHANDISERS COMPANY | 63941-192 | 63941-0192-01 |
| Extra Strength Pain Reliefacetaminophen | Acetaminophen 500 mg/1 | Capsule, Gelatin coatedOral | Geri-Care Pharmaceutical Corp | 57896-251 | 57896-0251-01 |
| Extra Strength pain reliefacetaminophen | Acetaminophen 500 mg/1 | Tablet, Film coatedOral | Rite Aid Corporation | 11822-5311 | 11822-5311-0211822-5311-05 |
| Extra Strength Pain Reliefacetaminophen | Acetaminophen 500 mg/1 | TabletOral | Geri-Care Pharmaceutical Corp | 57896-201 | 57896-0201-10 |
| Extra Strength Pain Reliefacetaminophen | Acetaminophen 500 mg/1 | TabletOral | Bryant Ranch Prepack | 63629-1516 | 63629-1516-0063629-1516-0163629-1516-02+7 more |
Other NDCs under 343
Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.
| Product | Strength | Form · route | Labeler | Product NDC |
|---|---|---|---|---|
| Acetaminophen | Acetaminophen 500 mg/1 | TabletOral | Preferrred Pharmaceuticals Inc. | 68788-8636 |
| Aspirin | Aspirin 325 mg/1 | TabletOral | Preferred Pharmaceuticals Inc. | 68788-8256 |
| Aspirin | Aspirin 81 mg/1 | Tablet, Delayed releaseOral | Preferred Pharmaceuticals Inc. | 68788-8598 |
| Aspirin Low Doseaspirin | Aspirin 81 mg/1 | Tablet, Delayed releaseOral | Preferred Pharmaceuticals Inc. | 68788-8334 |
| Childrens Acetaminophenacetaminophen | Acetaminophen 160 mg/5mL | SuspensionOral | Preferred Pharmaceuticals Inc. | 68788-8397 |
| Good Sense Childrens Pain and Feveracetaminophen | Acetaminophen 160 mg/5mL | SuspensionOral | Preferred Pharmaceuticals Inc. | 68788-8407 |
| good sense childrens pain and feveracetaminophen | Acetaminophen 160 mg/5mL | SuspensionOral | Preferred Pharmaceuticals Inc. | 68788-8477 |
| Good Sense Pain Reliefacetaminophen | Acetaminophen 500 mg/1 | TabletOral | Preferred Pharmaceuticals Inc. | 68788-8585 |