NDC 0135-0136
PANADOL Extra Strength
Acetaminophen
PANADOL Extra Strength is a Oral Tablet, Film Coated in the Human Otc Drug category. It is labeled and distributed by Glaxosmithkline Consumer Healthcare Holdings (us) Llc. The primary component is Acetaminophen.
| Product ID | 0135-0136_45fc4a8a-26e0-44a5-8033-50dfc8978a13 |
| NDC | 0135-0136 |
| Product Type | Human Otc Drug |
| Proprietary Name | PANADOL Extra Strength |
| Generic Name | Acetaminophen |
| Dosage Form | Tablet, Film Coated |
| Route of Administration | ORAL |
| Marketing Start Date | 2011-03-18 |
| Marketing End Date | 2019-05-31 |
| Marketing Category | OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL |
| Application Number | part343 |
| Labeler Name | GlaxoSmithKline Consumer Healthcare Holdings (US) LLC |
| Substance Name | ACETAMINOPHEN |
| Active Ingredient Strength | 500 mg/1 |
| NDC Exclude Flag | N |
Packaging
NDC 0135-0136-05
50 PACKET in 1 CARTON (0135-0136-05) > 2 TABLET, FILM COATED in 1 PACKET (0135-0136-09)
| Marketing Start Date | 2011-03-18 |
| NDC Exclude Flag | N |
| Sample Package? | N |
NDC SPL Data Element Entries
NDC 0135-0136-05 [00135013605]
PANADOL Extra Strength TABLET, FILM COATED
| Marketing Category | OTC monograph not final |
| Application Number | part343 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2011-03-18 |
| Marketing End Date | 2019-05-31 |
NDC 0135-0136-01 [00135013601]
PANADOL Extra Strength TABLET, FILM COATED
| Marketing Category | OTC monograph not final |
| Application Number | part343 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2011-04-18 |
| Marketing End Date | 2018-06-30 |
NDC 0135-0136-04 [00135013604]
PANADOL Extra Strength TABLET, FILM COATED
| Marketing Category | OTC monograph not final |
| Application Number | part343 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2011-03-18 |
| Marketing End Date | 2018-12-31 |
NDC 0135-0136-03 [00135013603]
PANADOL Extra Strength TABLET, FILM COATED
| Marketing Category | OTC monograph not final |
| Application Number | part343 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2011-03-18 |
| Marketing End Date | 2019-04-30 |
NDC 0135-0136-09 [00135013609]
PANADOL Extra Strength TABLET, FILM COATED
| Marketing Category | OTC monograph not final |
| Application Number | part343 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2012-09-10 |
| Marketing End Date | 2019-05-31 |
NDC 0135-0136-02 [00135013602]
PANADOL Extra Strength TABLET, FILM COATED
| Marketing Category | OTC monograph not final |
| Application Number | part343 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2011-03-18 |
| Marketing End Date | 2019-04-30 |
Drug Details
Active Ingredients
| Ingredient | Strength |
|---|---|
| ACETAMINOPHEN | 500 mg/1 |
OpenFDA Data
| SPL SET ID: | 62920a3f-c662-4db2-a4aa-8170a23ed3b6 |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI |
NDC Crossover Matching brand name "PANADOL Extra Strength" or generic name "Acetaminophen"
| NDC | Brand Name | Generic Name |
|---|---|---|
| 0135-0136 | PANADOL Extra Strength | PANADOL Extra Strength |
| 0135-0609 | PANADOL Extra Strength | PANADOL Extra Strength |
| 0121-0657 | Acetaminophen | Acetaminophen |
| 0113-7000 | Basic Care acetaminophen | Acetaminophen |
| 0113-7484 | basic care acetaminophen | Acetaminophen |
| 0113-7544 | Basic Care Acetaminophen | Acetaminophen |
| 0113-7130 | basic care childrens pain and fever | Acetaminophen |
| 0113-0020 | good sense childrens pain and fever | Acetaminophen |
| 0113-0212 | Good Sense Childrens Pain and Fever | Acetaminophen |
| 0113-0608 | good sense childrens pain and fever | Acetaminophen |
| 0113-0998 | Good Sense Childrens Pain and Fever | Acetaminophen |
| 0113-0161 | Good Sense pain and fever | Acetaminophen |
| 0113-0397 | Good Sense Pain and Fever | acetaminophen |
| 0113-0590 | Good Sense Pain and Fever | acetaminophen |
| 0113-0946 | good sense pain and fever | Acetaminophen |
| 0113-8959 | Good Sense Pain and Fever | Acetaminophen |
| 0113-0025 | Good Sense Pain Relief | Acetaminophen |
| 0113-0044 | Good Sense Pain Relief | Acetaminophen |
| 0113-0187 | good sense pain relief | Acetaminophen |
| 0113-0217 | good sense pain relief | Acetaminophen |
| 0113-0227 | Good Sense Pain Relief | Acetaminophen |
| 0113-0403 | good sense pain relief | Acetaminophen |
| 0113-0484 | Good Sense Pain Relief | Acetaminophen |
| 0113-0518 | good sense pain relief | Acetaminophen |
| 0113-0544 | good sense pain relief | Acetaminophen |
| 0113-1889 | good sense pain relief | acetaminophen |
| 0113-1975 | Good Sense Pain Relief | Acetaminophen |
| 0031-9301 | Robitussin Direct Sore Throat Pain | acetaminophen |
Trademark Results [PANADOL]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 PANADOL 87707023 5512890 Live/Registered |
GlaxoSmithKline Consumer Healthcare (UK) IP Limited 2017-12-04 |
 PANADOL 85678959 4408281 Live/Registered |
GLAXOSMITHKLINE CONSUMER HEALTHCARE (UK) IP LIMITED 2012-07-17 |
 PANADOL 73094226 1060597 Live/Registered |
STERLING DRUG INC. 1976-07-22 |
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