67877-322 : Tramadol Hcl and Acetaminophen Oral Tablet, Film Coated
NDC: | 67877-322 |
Labeler: | Ascend Laboratories, LLC |
Product Type: | Human Prescription Drug |
Drug Name: | Tramadol Hcl and Acetaminophen |
Dosage Form: | Oral Tablet, Film Coated |
Application #: | ANDA202076 |
Rev. Date: |
Appearance:
Markings: | alg;219 |
Shapes: |
Capsule |
Colors: |
Yellow |
Size (mm): | 15 |
Segments: * | 1 |
* Segments = the number of equally sized pieces which the pill can be broken into. In this case, a value of 1 indicates a solid pill with no score lines. |
NDC Package Codes:
- 67877-322-01: 100 TABLET, FILM COATED IN 1 BOTTLE (67877‑322‑01)
- 67877-322-05: 500 TABLET, FILM COATED IN 1 BOTTLE (67877‑322‑05)
- 67877-322-10: 1000 TABLET, FILM COATED IN 1 BOTTLE (67877‑322‑10)
Active Ingredients:
- Tramadol Hydrochloride
- Acetaminophen
Dosage Strength:
- 37.5 mg
- 325 mg
Inactive Ingredients:
- Crospovidone
- Hypromelloses
- Ferric Oxide Yellow
- Magnesium Stearate
- Cellulose, Microcrystalline
- Starch, Corn
- Polyethylene Glycols
- Sodium Starch Glycolate Type a Potato
- Titanium Dioxide
Pharmaceutical Classes:
- Full Opioid Agonists [MoA]
- Opioid Agonist [EPC]
Related Products:
Based on records with the same trade name.- 69844-049 Tramadol Hcl and Acetaminophen Oral Tablet, Film Coated by Graviti Pharmaceuticals Private Limited
NDC QR Code
Scan the QR code below to easily reference this data in the future:< Prev: 67877-321Next: 67877-390 >
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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.