Topcare All Day Pain Relief
- Product NDC
- 36800-140
- 11-digit product format
- 368000140
- Labeler code
- 36800
- Product ID
- 36800-140_9e77ead9-aabd-4ce0-a89d-86dd168c2663
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Naproxen sodium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Topco Associates LLC
- Application
- ANDA074661
- Marketing category
- ANDA
- Marketing start
- 2007-12-03
- Substance
- NAPROXEN SODIUM
- Active strength
- 220 mg/1
- Pharmacologic classes
- Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Topcare All Day Pain Relief
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| NAPROXEN SODIUM | 220 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 9TN87S3A3C |
| Rxcui | 849574 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 36800-140-82 | Topcare All Day Pain Relief | 200 in 1 BOTTLE | TABLET, FILM COATED | 200 | | 8 |
DailyMed Socrata Ingredients#
Ingredient, Type, UNII table| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|
| NAPROXEN SODIUM | ACTIVE INGREDIENT | 9TN87S3A3C | TOPCARE ALL DAY PAIN RELIEF (NAPROXEN SODIUM) TABLET, FILM COATED [TOPCO ASSOCIATES LLC] | 3 | |
| NAPROXEN | ACTIVE MOIETY | 57Y76R9ATQ | TOPCARE ALL DAY PAIN RELIEF (NAPROXEN SODIUM) TABLET, FILM COATED [TOPCO ASSOCIATES LLC] | 3 | |
| CELLULOSE, MICROCRYSTALLINE | INACTIVE INGREDIENT | OP1R32D61U | TOPCARE ALL DAY PAIN RELIEF (NAPROXEN SODIUM) TABLET, FILM COATED [TOPCO ASSOCIATES LLC] | 3 | |
| HYPROMELLOSES | INACTIVE INGREDIENT | 3NXW29V3WO | TOPCARE ALL DAY PAIN RELIEF (NAPROXEN SODIUM) TABLET, FILM COATED [TOPCO ASSOCIATES LLC] | 3 | |
| MAGNESIUM STEARATE | INACTIVE INGREDIENT | 70097M6I30 | TOPCARE ALL DAY PAIN RELIEF (NAPROXEN SODIUM) TABLET, FILM COATED [TOPCO ASSOCIATES LLC] | 3 | |
| POLYETHYLENE GLYCOLS | INACTIVE INGREDIENT | 3WJQ0SDW1A | TOPCARE ALL DAY PAIN RELIEF (NAPROXEN SODIUM) TABLET, FILM COATED [TOPCO ASSOCIATES LLC] | 3 | |
| POVIDONES | INACTIVE INGREDIENT | FZ989GH94E | TOPCARE ALL DAY PAIN RELIEF (NAPROXEN SODIUM) TABLET, FILM COATED [TOPCO ASSOCIATES LLC] | 3 | |
| TALC | INACTIVE INGREDIENT | 7SEV7J4R1U | TOPCARE ALL DAY PAIN RELIEF (NAPROXEN SODIUM) TABLET, FILM COATED [TOPCO ASSOCIATES LLC] | 3 | |
| TITANIUM DIOXIDE | INACTIVE INGREDIENT | 15FIX9V2JP | TOPCARE ALL DAY PAIN RELIEF (NAPROXEN SODIUM) TABLET, FILM COATED [TOPCO ASSOCIATES LLC] | 3 | |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 36800-140 | TOPCARE ALL DAY PAIN RELIEF (NAPROXEN SODIUM) TABLET, FILM COATED [TOPCO ASSOCIATES LLC] | 8 | Current NDC, Legacy NDC, 1 package rows | 20240426_f151d48d-a8f7-484e-9ce8-6b2e8dd1093f.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 36800-140-82 | 36800014082 | 200 TABLET, FILM COATED in 1 BOTTLE (36800-140-82) | 2007-12-03 | 0000-00-00 | No | No | Current |