Mucus Relief - Guaifenesin 1200 mg / 1 Tablet 14 Blister Pack
Reference details for licensed healthcare facility review and verification.
| NDC 11 | 00536-1392-88 |
|---|---|
| Product NDC | 00536-1392 |
| Generic Drug Name | Guaifenesin |
| Brand Name | Mucus Relief |
| Manufacturer | Rugby Laboratories, Inc. |
| Strength | 1200 mg / 1 |
| Dosage Form | Tablet |
| Drug Type | Oral |
| Package Quantity | 14 Blister Pack |
| Package Description | 14 BLISTER PACK in 1 CARTON (0536-1392-88) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK |
| Active Ingredients | Guaifenesin |
| Marketing Category | ANDA |
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NDC snapshot
Guaifenesin 1200 mg / 1 Tablet is tracked under NDC 00536-1392-88 and rolls up into product family 00536-1392. Use this page to review package-level identifiers before comparing related family pages or starting a quote review.
- Package configuration: 14 Blister Pack.
- Manufacturer: Rugby Laboratories, Inc..
- Dosage form: Tablet.
- Family size: 1 indexed presentation.
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Official references
Use official labeling and directory references to confirm presentation details while your team reviews the PRN catalog entry and related sourcing paths.
Potential alternatives with matching presentation
Open the comparison hub or review package-level listings from 6 product-NDC families with matching normalized presentation details. Review each product detail page before treating any item as a true alternative.
Mucus Relief - Guaifenesin 1200 mg / 1 Tablet 14 Blister Pack, NDC 00536-1392-88, is a Rugby Laboratories, Inc. 1200 mg / 1 tablet presentation packaged as 14 Blister Pack.
NDC search formats
- Canonical NDC 11: 00536-1392-88
- Digits-only NDC 11: 00536139288
- Possible 10-digit display format: 0536-1392-88 (0536139288)
Helpful product links
- Search by brand name: Mucus Relief
- NDC 11: 00536-1392-88
- Product family NDC: 00536-1392
- VA classification code: RE302
- VA classification code description: NON-OPIOID-CONTAINING ANTITUSSIVES/EXPECTORANTS
- CMOP ID: G0161
- VUID: 4007875