63824-023 : Mucinex 1200 mg 12 Hr Extended Release Tablet
| NDC: | 63824-023 |
| Labeler: | Reckitt Benckiser LLC |
| Product Type: | Human OTC Drug |
| Drug Name: |  Mucinex Maximum Strength |
| Dosage Form: | Oral Tablet, Extended Release |
| Application #: | NDA021282 |
| Rev. Date: |
Appearance:
| Markings: | Mucinex;1200 |
| Shapes: |
Oval |
| Colors: |
 White |
| Size (mm): | 22 |
| 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:
- 63824-023-02: 1 POUCH IN 1 CARTON (63824‑023‑02) > 1 TABLET, EXTENDED RELEASE IN 1 POUCH
- 63824-023-07: 1 BLISTER PACK IN 1 CARTON (63824‑023‑07) > 7 TABLET, EXTENDED RELEASE IN 1 BLISTER PACK
- 63824-023-14: 1 BOTTLE IN 1 CARTON (63824‑023‑14) > 14 TABLET, EXTENDED RELEASE IN 1 BOTTLE
- 63824-023-18: 2 BLISTER PACK IN 1 CARTON (63824‑023‑18) > 9 TABLET, EXTENDED RELEASE IN 1 BLISTER PACK
- 63824-023-28: 1 BOTTLE IN 1 CARTON (63824‑023‑28) > 28 TABLET, EXTENDED RELEASE IN 1 BOTTLE
- 63824-023-35: 1 BLISTER PACK IN 1 CARTON (63824‑023‑35) > 14 TABLET, EXTENDED RELEASE IN 1 BLISTER PACK
- 63824-023-36: 2 BLISTER PACK IN 1 CARTON (63824‑023‑36) > 14 TABLET, EXTENDED RELEASE IN 1 BLISTER PACK
- 63824-023-43: 1 BOTTLE IN 1 BLISTER PACK (63824‑023‑43) > 42 TABLET, EXTENDED RELEASE IN 1 BOTTLE
- 63824-023-45: 1 BOTTLE IN 1 BLISTER PACK (63824‑023‑45) > 44 TABLET, EXTENDED RELEASE IN 1 BOTTLE
- 63824-023-46: 3 BLISTER PACK IN 1 CARTON (63824‑023‑46) > 14 TABLET, EXTENDED RELEASE IN 1 BLISTER PACK
- 63824-023-48: 4 BLISTER PACK IN 1 CARTON (63824‑023‑48) > 12 TABLET, EXTENDED RELEASE IN 1 BLISTER PACK
- 63824-023-56: 4 BLISTER PACK IN 1 CARTON (63824‑023‑56) > 14 TABLET, EXTENDED RELEASE IN 1 BLISTER PACK
- 63824-023-71: 24 POUCH IN 1 CARTON (63824‑023‑71) > 1 TABLET, EXTENDED RELEASE IN 1 POUCH
Active Ingredients:
- Guaifenesin
Dosage Strength:
- 1200 mg
Inactive Ingredients:
- Carbomer Homopolymer Type B (Allyl Pentaerythritol Crosslinked)
- Fd&c Blue No. 1
- Aluminum Oxide
- Hypromelloses
- Magnesium Stearate
- Cellulose, Microcrystalline
Pharmaceutical Classes:
- Decreased Respiratory Secretion Viscosity [PE]
- Expectorant [EPC]
- Increased Respiratory Secretions [PE]
Related Products:
Based on records with the same trade name.- 63824-008 Mucinex 600 mg 12 Hr Extended Release Tablet by Reckitt Benckiser LLC
- 17856-0008 Mucinex 600 mg 12 Hr Extended Release Tablet by Atlantic Biologicals Corps
- 21695-870 Mucinex 600 mg 12 Hr Extended Release Tablet by Rebel Distributors Corp
- 50090-0818 Mucinex 600 mg Oral Tablet, Extended Release by A-s Medication Solutions
- 50090-1340 Mucinex 600 mg Oral Tablet, Extended Release by A-s Medication Solutions
- 50090-2300 Mucinex 600 mg Oral Tablet, Extended Release by A-s Medication Solutions
- 50090-2380 Mucinex 600 mg Oral Tablet, Extended Release by A-s Medication Solutions
- 53808-0871 Mucinex 600 mg Oral Tablet, Extended Release by State of Florida Doh Central Pharmacy
- 54569-5463 Mucinex 600 mg Oral Tablet, Extended Release by A-s Medication Solutions
- 54868-4750 Mucinex 600 mg 12 Hr Extended Release Tablet by Physicians Total Care, Inc.
- 55045-3143 Mucinex 600 mg 12 Hr Extended Release Tablet by Dispensing Solutions, Inc.
- 55154-4680 Mucinex 600 mg Oral Tablet, Extended Release by Cardinal Health
- 55154-7776 Mucinex 600 mg 12 Hr Extended Release Tablet by Cardinal Health
- 55154-7777 Mucinex 600 mg 12 Hr Extended Release Tablet by Cardinal Health
- 55289-087 Mucinex 600 mg Oral Tablet, Extended Release by Pd-rx Pharmaceuticals, Inc.
- 55700-489 Mucinex 600 mg Oral Tablet, Extended Release by Lake Erie Medical Dba Quality Care Products LLC
- 61919-651 Mucinex 600 mg Oral Tablet, Extended Release by Direct Rx
- 63187-954 Mucinex 600 mg Oral Tablet, Extended Release by Proficient Rx Lp
- 63629-7115 Mucinex 600 mg Oral Tablet, Extended Release by Bryant Ranch Prepack
- 63629-7886 Mucinex 600 mg Oral Tablet, Extended Release by Bryant Ranch Prepack
- More related products ...
NDC QR Code
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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.